Name

CTD Gene-Disease Associations Dataset

From Comparative Toxicogenomics Database

Disease-gene interactions from manually curated literature

DISEASES Curated Gene-Disease Association Evidence Scores Dataset (Archived)

From DISEASES

Disease gene evidence scores by manual literature curation

DISEASES Experimental Gene-Disease Association Evidence Scores Dataset (Archived)

From DISEASES

Disease gene evidence scores by integrating experimental data (GWAS)

DISEASES Text-mining Gene-Disease Association Evidence Scores Dataset (Archived)

From DISEASES

Gene-disease co-occurrence scores from text-mining biomedical abstracts

GAD Gene-Disease Associations Dataset

From Genetic Association Database

Gene-disease associations curated from genetic association studies

GAD High Level Gene-Disease Associations Dataset

From Genetic Association Database

Gene-disease associations curated from genetic association studies

GWASdb SNP-Disease Associations Dataset

From GWASdb

SNP-disease association p-values curated from published GWAS

HPO Gene-Disease Associations Dataset

From Human Phenotype Ontology

Phenotype-causing gene mutations of human phenotypes from disease knowledgebases

OMIM Gene-Disease Associations Dataset

From Online Mendelian Inheritance in Man

Disease- or phenotype-causing gene mutations for heritable human diseases or phenotypes curated from biomedical publications

PhosphoSitePlus Phosphosite-Disease Associations Dataset

From PhosphoSitePlus

Disease-phosphosite associations curated from literature

DisGeNET Gene-Disease Associations Dataset

From DisGeNET

Gene-disease associations sourced from curated repositories, GWAS catalogues, animal models and the scientific literature

DISEASES Curated Gene-Disease Association Evidence Scores 2025 Dataset

From DISEASES

Disease gene evidence scores by manual literature curation

DISEASES Experimental Gene-Disease Association Evidence Scores 2025 Dataset

From DISEASES

Disease gene evidence scores by integrating experimental data (GWAS)

DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 Dataset

From DISEASES

Gene-disease co-occurrence scores from text-mining biomedical abstracts

LOC105378951 Gene

collagen alpha-1(III) chain-like

LOC101930347 Gene

collagen alpha-2(I) chain-like

COL14A1 Gene

collagen, type XIV, alpha 1

This gene encodes the alpha chain of type XIV collagen, a member of the FACIT (fibril-associated collagens with interrupted triple helices) collagen family. Type XIV collagen interacts with the fibril surface and is involved in the regulation of fibrillogenesis. [provided by RefSeq, Jan 2013]

LOC105369637 Gene

collagen alpha-1(I) chain-like

LOC105370705 Gene

collagen alpha-2(I) chain-like

COL27A1 Gene

collagen, type XXVII, alpha 1

This gene encodes a member of the fibrillar collagen family, and plays a role during the calcification of cartilage and the transition of cartilage to bone. The encoded protein product is a preproprotein. It includes an N-terminal signal peptide, which is followed by an N-terminal propetide, mature peptide and a C-terminal propeptide. The N-terminal propeptide contains thrombospondin N-terminal-like and laminin G-like domains. The mature peptide is a major triple-helical region. The C-terminal propeptide, also known as COLFI domain, plays crucial roles in tissue growth and repair. Mutations in this gene cause Steel syndrome. Alternatively spliced transcript variants have been found, but the full-length nature of some variants has not been determined. [provided by RefSeq, Sep 2014]

LOC101060328 Gene

collagen alpha-1(I) chain-like

COL9A2 Gene

collagen, type IX, alpha 2

This gene encodes one of the three alpha chains of type IX collagen, the major collagen component of hyaline cartilage. Type IX collagen, a heterotrimeric molecule, is usually found in tissues containing type II collagen, a fibrillar collagen. This chain is unusual in that, unlike the other two type IX alpha chains, it contains a covalently attached glycosaminoglycan side chain. Mutations in this gene are associated with multiple epiphyseal dysplasia. [provided by RefSeq, Jul 2008]

COL9A3 Gene

collagen, type IX, alpha 3

This gene encodes one of the three alpha chains of type IX collagen, the major collagen component of hyaline cartilage. Type IX collagen, a heterotrimeric molecule, is usually found in tissues containing type II collagen, a fibrillar collagen. Mutations in this gene are associated with multiple epiphyseal dysplasia type 3. [provided by RefSeq, Jan 2010]

COL9A1 Gene

collagen, type IX, alpha 1

This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20%) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

LOC100420255 Gene

collagen, type XXII, alpha 1 pseudogene

LOC105376747 Gene

collagen alpha-3(IX) chain-like

COL1AR Gene

collagen, type I, alpha, receptor

COL1A2 Gene

collagen, type I, alpha 2

This gene encodes the pro-alpha2 chain of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity. Three transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]

LOC101929990 Gene

collagen alpha-1(XXVII) chain-like

COL6A1 Gene

collagen, type VI, alpha 1

The collagens are a superfamily of proteins that play a role in maintaining the integrity of various tissues. Collagens are extracellular matrix proteins and have a triple-helical domain as their common structural element. Collagen VI is a major structural component of microfibrils. The basic structural unit of collagen VI is a heterotrimer of the alpha1(VI), alpha2(VI), and alpha3(VI) chains. The alpha2(VI) and alpha3(VI) chains are encoded by the COL6A2 and COL6A3 genes, respectively. The protein encoded by this gene is the alpha 1 subunit of type VI collagen (alpha1(VI) chain). Mutations in the genes that code for the collagen VI subunits result in the autosomal dominant disorder, Bethlem myopathy. [provided by RefSeq, Jul 2008]

COL6A2 Gene

collagen, type VI, alpha 2

This gene encodes one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The product of this gene contains several domains similar to von Willebrand Factor type A domains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in this gene are associated with Bethlem myopathy and Ullrich scleroatonic muscular dystrophy. Three transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]

COL6A5 Gene

collagen, type VI, alpha 5

This gene encodes a member of the collagen superfamily of proteins. The encoded protein contains multiple von Willebrand factor A-like domains and may interact with the alpha 1 and alpha 2 chains of collagen VI to form the complete collagen VI trimer. Polymorphisms in this gene may be linked to dermal phenotypes, such as eczema. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]

LOC105377621 Gene

collagen alpha-2(I) chain-like

LOC105379509 Gene

fibril-forming collagen alpha chain-like

COL17A1 Gene

collagen, type XVII, alpha 1

This gene encodes the alpha chain of type XVII collagen. Unlike most collagens, collagen XVII is a transmembrane protein. Collagen XVII is a structural component of hemidesmosomes, multiprotein complexes at the dermal-epidermal basement membrane zone that mediate adhesion of keratinocytes to the underlying membrane. Mutations in this gene are associated with both generalized atrophic benign and junctional epidermolysis bullosa. Two homotrimeric forms of type XVII collagen exist. The full length form is the transmembrane protein. A soluble form, referred to as either ectodomain or LAD-1, is generated by proteolytic processing of the full length form. [provided by RefSeq, Jul 2008]

LOC105373619 Gene

collagen alpha-1(XI) chain-like

LOC101059944 Gene

collagen alpha-1(III) chain-like

LOC105373316 Gene

collagen alpha-4(IV) chain-like

LOC105370367 Gene

collagen alpha-2(VIII) chain-like

LOC105370368 Gene

collagen alpha-2(I) chain-like

LOC645544 Gene

cuticle collagen 7-like

LOC387720 Gene

collagen alpha-1(X) chain

LOC105375661 Gene

collagen alpha-1(I) chain-like

COL21A1 Gene

collagen, type XXI, alpha 1

This gene encodes the alpha chain of type XXI collagen, a member of the FACIT (fibril-associated collagens with interrupted helices) collagen family. Type XXI collagen is localized to tissues containing type I collagen and maintains the integrity of the extracellular matrix. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

COL18A1 Gene

collagen, type XVIII, alpha 1

This gene encodes the alpha chain of type XVIII collagen. This collagen is one of the multiplexins, extracellular matrix proteins that contain multiple triple-helix domains (collagenous domains) interrupted by non-collagenous domains. A long isoform of the protein has an N-terminal domain that is homologous to the extracellular part of frizzled receptors. Proteolytic processing at several endogenous cleavage sites in the C-terminal domain results in production of endostatin, a potent antiangiogenic protein that is able to inhibit angiogenesis and tumor growth. Mutations in this gene are associated with Knobloch syndrome. The main features of this syndrome involve retinal abnormalities, so type XVIII collagen may play an important role in retinal structure and in neural tube closure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]

COL28A1 Gene

collagen, type XXVIII, alpha 1

COL28A1 belongs to a class of collagens containing von Willebrand factor (VWF; MIM 613160) type A (VWFA) domains (Veit et al., 2006 [PubMed 16330543]).[supplied by OMIM, Nov 2010]

COL11A1 Gene

collagen, type XI, alpha 1

This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Mutations in this gene are associated with type II Stickler syndrome and with Marshall syndrome. A single-nucleotide polymorphism in this gene is also associated with susceptibility to lumbar disc herniation. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009]

COL11A2 Gene

collagen, type XI, alpha 2

This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]

LOC105376684 Gene

collagen alpha-2(I) chain-like

FCN3 Gene

ficolin (collagen/fibrinogen domain containing) 3

Ficolins are a group of proteins which consist of a collagen-like domain and a fibrinogen-like domain. In human serum, there are two types of ficolins, both of which have lectin activity. The protein encoded by this gene is a thermolabile beta-2-macroglycoprotein found in all human serum and is a member of the ficolin/opsonin p35 lectin family. The protein, which was initially identified based on its reactivity with sera from patients with systemic lupus erythematosus, has been shown to have a calcium-independent lectin activity. The protein can activate the complement pathway in association with MASPs and sMAP, thereby aiding in host defense through the activation of the lectin pathway. Alternative splicing occurs at this locus and two variants, each encoding a distinct isoform, have been identified. [provided by RefSeq, Jul 2008]

FCN2 Gene

ficolin (collagen/fibrinogen domain containing lectin) 2

The product of this gene belongs to the ficolin family of proteins. This family is characterized by the presence of a leader peptide, a short N-terminal segment, followed by a collagen-like region, and a C-terminal fibrinogen-like domain. This gene is predominantly expressed in the liver, and has been shown to have carbohydrate binding and opsonic activities. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

FCN1 Gene

ficolin (collagen/fibrinogen domain containing) 1

The ficolin family of proteins are characterized by the presence of a leader peptide, a short N-terminal segment, followed by a collagen-like region, and a C-terminal fibrinogen-like domain. The collagen-like and the fibrinogen-like domains are also found separately in other proteins such as complement protein C1q, C-type lectins known as collectins, and tenascins. However, all these proteins recognize different targets, and are functionally distinct. Ficolin 1 encoded by FCN1 is predominantly expressed in the peripheral blood leukocytes, and has been postulated to function as a plasma protein with elastin-binding activity. [provided by RefSeq, Jul 2008]

LOC105371935 Gene

collagen alpha-4(IV) chain-like

LOC105372231 Gene

collagen alpha-1(III) chain-like

COL22A1 Gene

collagen, type XXII, alpha 1

This gene encodes member of the collagen family which is thought to contribute to the stabilization of myotendinous junctions and strengthen skeletal muscle attachments during contractile activity. It belongs to the fibril-associated collagens with interrupted triple helix (FACIT) subset of the collagen superfamily, which associate with collagen fibers through their C-terminal collagenous domains and mediate protein-protein interactions through their N-terminal noncollagenous domains. The encoded protein is deposited in the basement membrane zone of the myotendinous junction which is present only at the tissue junctions of muscles, tendons, the heart, articular cartilage, and skin. A knockdown of the orthologous zebrafish gene induces a muscular dystrophy by disruption of the myotendinous junction. [provided by RefSeq, May 2017]

COL5A2 Gene

collagen, type V, alpha 2

This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. Mutations in this gene are associated with Ehlers-Danlos syndrome, types I and II. [provided by RefSeq, Jul 2008]

COL5A3 Gene

collagen, type V, alpha 3

This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. Mutations in this gene are thought to be responsible for the symptoms of a subset of patients with Ehlers-Danlos syndrome type III. Messages of several sizes can be detected in northern blots but sequence information cannot confirm the identity of the shorter messages. [provided by RefSeq, Jul 2008]

COL5A1 Gene

collagen, type V, alpha 1

This gene encodes an alpha chain for one of the low abundance fibrillar collagens. Fibrillar collagen molecules are trimers that can be composed of one or more types of alpha chains. Type V collagen is found in tissues containing type I collagen and appears to regulate the assembly of heterotypic fibers composed of both type I and type V collagen. This gene product is closely related to type XI collagen and it is possible that the collagen chains of types V and XI constitute a single collagen type with tissue-specific chain combinations. The encoded procollagen protein occurs commonly as the heterotrimer pro-alpha1(V)-pro-alpha1(V)-pro-alpha2(V). Mutations in this gene are associated with Ehlers-Danlos syndrome, types I and II. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]

LOC100506596 Gene

fibril-forming collagen alpha chain

LOC105375938 Gene

collagen alpha-1(I) chain-like

COL12A1 Gene

collagen, type XII, alpha 1

This gene encodes the alpha chain of type XII collagen, a member of the FACIT (fibril-associated collagens with interrupted triple helices) collagen family. Type XII collagen is a homotrimer found in association with type I collagen, an association that is thought to modify the interactions between collagen I fibrils and the surrounding matrix. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

COL6A4P1 Gene

collagen, type VI, alpha 4 pseudogene 1

This transcribed pseudogene represents the 5' end of a presumed ortholog to a mouse gene which encodes a collagen VI alpha 4 chain protein (GeneID 68553). No complete ORF of comparable size to the mouse protein is found in this gene. The predicted protein lacks a signal peptide; however, this truncated collagen polypeptide may have achieved a different function as suggested by PubMed ID: 18622395. Evidence of in vivo translation is incomplete. A large chromosome break separates this pseudogene from the 3' end of the presumed ortholog (COL6A4P2, GeneID 646300) which is located downstream at chromosome 3q21.3. [provided by RefSeq, Jun 2009]

LOC105376068 Gene

collagen alpha-1(I) chain-like

COL6A4P2 Gene

collagen, type VI, alpha 4 pseudogene 2

This transcribed pseudogene represents the 3' end of a presumed ortholog to a mouse gene which encodes a collagen VI alpha 4 chain protein (GeneID 68553). The predicted ORF contains multiple premature stop codons. A large chromosome break separates this pseudogene from the 5' end of the presumed ortholog (DVWA, GeneID 344875) which is located upstream at chromosome 3p24.3. [provided by RefSeq, Jun 2009]

COL25A1 Gene

collagen, type XXV, alpha 1

This gene encodes a brain-specific membrane associated collagen. A product of proteolytic processing of the encoded protein, CLAC (collagenous Alzheimer amyloid plaque component), binds to amyloid beta-peptides found in Alzheimer amyloid plaques but CLAC inhibits rather than facilitates amyloid fibril elongation (PMID: 16300410). A study of over-expression of this collagen in mice, however, found changes in pathology and behavior suggesting that the encoded protein may promote amyloid plaque formation (PMID: 19548013). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

COL2A1 Gene

collagen, type II, alpha 1

This gene encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene. [provided by RefSeq, Jul 2008]

COLQ Gene

collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase

This gene encodes the subunit of a collagen-like molecule associated with acetylcholinesterase in skeletal muscle. Each molecule is composed of three identical subunits. Each subunit contains a proline-rich attachment domain (PRAD) that binds an acetylcholinesterase tetramer to anchor the catalytic subunit of the enzyme to the basal lamina. Mutations in this gene are associated with endplate acetylcholinesterase deficiency. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

LOC101929301 Gene

collagen alpha-1(I) chain-like

COL15A1 Gene

collagen, type XV, alpha 1

This gene encodes the alpha chain of type XV collagen, a member of the FACIT collagen family (fibril-associated collagens with interrupted helices). Type XV collagen has a wide tissue distribution but the strongest expression is localized to basement membrane zones so it may function to adhere basement membranes to underlying connective tissue stroma. The proteolytically produced C-terminal fragment of type XV collagen is restin, a potentially antiangiogenic protein that is closely related to endostatin. Mouse studies have shown that collagen XV deficiency is associated with muscle and microvessel deterioration. [provided by RefSeq, May 2013]

LOC105377821 Gene

collagen alpha-2(I) chain-like

LOC105379421 Gene

collagen alpha-1(III) chain-like

LOC101059958 Gene

collagen alpha-1(II) chain-like

LOC105379575 Gene

collagen alpha-2(IV) chain-like

COL26A1 Gene

collagen, type XXVI, alpha 1

This gene encodes a protein containing an emilin domain and two collagen stretches. This gene may be associated with aspirin-intolerant asthma. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]

LOC105371095 Gene

collagen alpha-3(IX) chain-like

COL8A2 Gene

collagen, type VIII, alpha 2

This gene encodes the alpha 2 chain of type VIII collagen. This protein is a major component of the basement membrane of the corneal endothelium and forms homo- or heterotrimers with alpha 1 (VIII) type collagens. Defects in this gene are associated with Fuchs endothelial corneal dystrophy and posterior polymorphous corneal dystrophy type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]

COL8A1 Gene

collagen, type VIII, alpha 1

This gene encodes one of the two alpha chains of type VIII collagen. The gene product is a short chain collagen and a major component of the basement membrane of the corneal endothelium. The type VIII collagen fibril can be either a homo- or a heterotrimer. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Dec 2011]

COL16A1 Gene

collagen, type XVI, alpha 1

This gene encodes the alpha chain of type XVI collagen, a member of the FACIT collagen family (fibril-associated collagens with interrupted helices). Members of this collagen family are found in association with fibril-forming collagens such as type I and II, and serve to maintain the integrity of the extracellular matrix. High levels of type XVI collagen have been found in fibroblasts and keratinocytes, and in smooth muscle and amnion. [provided by RefSeq, Jul 2008]

LOC105373982 Gene

collagen alpha-1(III) chain-like

CCBE1 Gene

collagen and calcium binding EGF domains 1

This gene is thought to function in extracellular matrix remodeling and migration. It is predominantly expressed in the ovary, but down regulated in ovarian cancer cell lines and primary carcinomas, suggesting its role as a tumour suppressor. Mutations in this gene have been associated with Hennekam lymphangiectasia-lymphedema syndrome, a generalized lymphatic dysplasia in humans. [provided by RefSeq, Mar 2010]

COLGALT2 Gene

collagen beta(1-O)galactosyltransferase 2

Predicted to enable procollagen galactosyltransferase activity. Predicted to be involved in collagen fibril organization. Predicted to be located in endoplasmic reticulum lumen. [provided by Alliance of Genome Resources, Mar 2025]

COLGALT1 Gene

collagen beta(1-O)galactosyltransferase 1

The protein encoded by this gene is one of two enzymes that transfers galactose moieties to hydroxylysine residues of collagen and mannose binding lectin. This gene is constitutively expressed and encodes a soluble protein that localizes to the endoplasmic reticulum. [provided by RefSeq, Dec 2015]

LOC105379779 Gene

collagen alpha-1(I) chain-like

ADIPOQ Gene

adiponectin, C1Q and collagen domain containing

This gene is expressed in adipose tissue exclusively. It encodes a protein with similarity to collagens X and VIII and complement factor C1q. The encoded protein circulates in the plasma and is involved with metabolic and hormonal processes. Mutations in this gene are associated with adiponectin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Apr 2010]

LOC102725144 Gene

collagen alpha-1(III) chain-like

CTHRC1 Gene

collagen triple helix repeat containing 1

This locus encodes a protein that may play a role in the cellular response to arterial injury through involvement in vascular remodeling. Mutations at this locus have been associated with Barrett esophagus and esophageal adenocarcinoma. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2012]

LOC101928841 Gene

collagen alpha-1(II) chain-like

LOC101927503 Gene

collagen alpha-1(III) chain-like

LOC105375304 Gene

collagen alpha-1(I) chain-like

COL20A1 Gene

collagen, type XX, alpha 1

Predicted to be located in endoplasmic reticulum lumen and extracellular region. Predicted to be part of collagen trimer. Predicted to be active in collagen-containing extracellular matrix. [provided by Alliance of Genome Resources, Mar 2025]

SERPINH1 Gene

serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)

This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The encoded protein is localized to the endoplasmic reticulum and plays a role in collagen biosynthesis as a collagen-specific molecular chaperone. Autoantibodies to the encoded protein have been found in patients with rheumatoid arthritis. Expression of this gene may be a marker for cancer, and nucleotide polymorphisms in this gene may be associated with preterm birth caused by preterm premature rupture of membranes. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, May 2011]

COL7A1 Gene

collagen, type VII, alpha 1

This gene encodes the alpha chain of type VII collagen. The type VII collagen fibril, composed of three identical alpha collagen chains, is restricted to the basement zone beneath stratified squamous epithelia. It functions as an anchoring fibril between the external epithelia and the underlying stroma. Mutations in this gene are associated with all forms of dystrophic epidermolysis bullosa. In the absence of mutations, however, an acquired form of this disease can result from an autoimmune response made to type VII collagen. [provided by RefSeq, Jul 2008]

COL4A6 Gene

collagen, type IV, alpha 6

This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene, alpha 5 type IV collagen, so that the gene pair shares a common promoter. Deletions in the alpha 5 gene that extend into the alpha 6 gene result in diffuse leiomyomatosis accompanying the X-linked Alport syndrome caused by the deletion in the alpha 5 gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2013]

COL4A5 Gene

collagen, type IV, alpha 5

This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]

COL4A4 Gene

collagen, type IV, alpha 4

This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. This particular collagen IV subunit, however, is only found in a subset of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease). Two transcripts, differing only in their transcription start sites, have been identified for this gene and, as is common for collagen genes, multiple polyadenylation sites are found in the 3' UTR. [provided by RefSeq, Jul 2008]

COL4A3 Gene

collagen, type IV, alpha 3 (Goodpasture antigen)

Type IV collagen, the major structural component of basement membranes, is a multimeric protein composed of 3 alpha subunits. These subunits are encoded by 6 different genes, alpha 1 through alpha 6, each of which can form a triple helix structure with 2 other subunits to form type IV collagen. This gene encodes alpha 3. In the Goodpasture syndrome, autoantibodies bind to the collagen molecules in the basement membranes of alveoli and glomeruli. The epitopes that elicit these autoantibodies are localized largely to the non-collagenous C-terminal domain of the protein. A specific kinase phosphorylates amino acids in this same C-terminal region and the expression of this kinase is upregulated during pathogenesis. This gene is also linked to an autosomal recessive form of Alport syndrome. The mutations contributing to this syndrome are also located within the exons that encode this C-terminal region. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. [provided by RefSeq, Jun 2010]

COL4A2 Gene

collagen, type IV, alpha 2

This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. The C-terminal portion of the protein, known as canstatin, is an inhibitor of angiogenesis and tumor growth. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. [provided by RefSeq, Jul 2008]

COL4A1 Gene

collagen, type IV, alpha 1

This gene encodes a type IV collagen alpha protein. Type IV collagen proteins are integral components of basement membranes. This gene shares a bidirectional promoter with a paralogous gene on the opposite strand. The protein consists of an amino-terminal 7S domain, a triple-helix forming collagenous domain, and a carboxy-terminal non-collagenous domain. It functions as part of a heterotrimer and interacts with other extracellular matrix components such as perlecans, proteoglycans, and laminins. In addition, proteolytic cleavage of the non-collagenous carboxy-terminal domain results in a biologically active fragment known as arresten, which has anti-angiogenic and tumor suppressor properties. Mutations in this gene cause porencephaly, cerebrovascular disease, and renal and muscular defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]

LOC105373289 Gene

collagen alpha-1(III) chain-like

COL19A1 Gene

collagen, type XIX, alpha 1

This gene encodes the alpha chain of type XIX collagen, a member of the FACIT collagen family (fibril-associated collagens with interrupted helices). Although the function of this collagen is not known, other members of this collagen family are found in association with fibril-forming collagens such as type I and II, and serve to maintain the integrity of the extracellular matrix. The transcript produced from this gene has an unusually large 3' UTR which has not been completely sequenced. [provided by RefSeq, Jul 2008]

COL10A1 Gene

collagen, type X, alpha 1

This gene encodes the alpha chain of type X collagen, a short chain collagen expressed by hypertrophic chondrocytes during endochondral ossification. Unlike type VIII collagen, the other short chain collagen, type X collagen is a homotrimer. Mutations in this gene are associated with Schmid type metaphyseal chondrodysplasia (SMCD) and Japanese type spondylometaphyseal dysplasia (SMD). [provided by RefSeq, Jul 2008]

COL11A2P1 Gene

collagen, type XI, alpha 2 pseudogene 1

COL1A1 Gene

collagen, type I, alpha 1

This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]

COL6A3 Gene

collagen, type VI, alpha 3

This gene encodes the alpha-3 chain, one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The alpha-3 chain of type VI collagen is much larger than the alpha-1 and -2 chains. This difference in size is largely due to an increase in the number of subdomains, similar to von Willebrand Factor type A domains, that are found in the amino terminal globular domain of all the alpha chains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in the type VI collagen genes are associated with Bethlem myopathy, a rare autosomal dominant proximal myopathy with early childhood onset. Mutations in this gene are also a cause of Ullrich congenital muscular dystrophy, also referred to as Ullrich scleroatonic muscular dystrophy, an autosomal recessive congenital myopathy that is more severe than Bethlem myopathy. Multiple transcript variants have been identified, but the full-length nature of only some of these variants has been described. [provided by RefSeq, Jun 2009]

COL6A6 Gene

collagen, type VI, alpha 6

This gene encodes a large protein that contains multiple von Willebrand factor domains and forms a component of the basal lamina of epithelial cells. This protein may regulate epithelial cell-fibronectin interactions. Variation in this gene may be implicated in skin diseases. [provided by RefSeq, May 2017]

COL4A3BP Gene

collagen, type IV, alpha 3 (Goodpasture antigen) binding protein

This gene encodes a kinase that specifically phosphorylates the N-terminal region of the non-collagenous domain of the alpha 3 chain of type IV collagen, known as the Goodpasture antigen. Goodpasture disease is the result of an autoimmune response directed at this antigen. One isoform of this protein is also involved in ceramide intracellular transport. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

COL23A1 Gene

collagen, type XXIII, alpha 1

COL23A1 is a member of the transmembrane collagens, a subfamily of the nonfibrillar collagens that contain a single pass hydrophobic transmembrane domain (Banyard et al., 2003 [PubMed 12644459]).[supplied by OMIM, Mar 2008]

LOC102723531 Gene

collagen alpha-1(I) chain-like

LOC102725000 Gene

collagen alpha-2(V) chain-like

LOC105376877 Gene

collagen alpha-2(IV) chain-like

LOC105379637 Gene

collagen alpha-2(IV) chain-like

LOC105374379 Gene

collagen alpha-1(X) chain-like

COL13A1 Gene

collagen, type XIII, alpha 1

This gene encodes the alpha chain of one of the nonfibrillar collagens. The function of this gene product is not known, however, it has been detected at low levels in all connective tissue-producing cells so it may serve a general function in connective tissues. Unlike most of the collagens, which are secreted into the extracellular matrix, collagen XIII contains a transmembrane domain and the protein has been localized to the plasma membrane. The transcripts for this gene undergo complex and extensive splicing involving at least eight exons. Like other collagens, collagen XIII is a trimer; it is not known whether this trimer is composed of one or more than one alpha chain isomer. A number of alternatively spliced transcript variants have been described, but the full length nature of some of them has not been determined. [provided by RefSeq, Jul 2008]

LOC105379510 Gene

collagen alpha-1(II) chain-like

LOC105371405 Gene

collagen alpha-1(XIII) chain

LOC101059906 Gene

collagen alpha-2(IV) chain-like

LOC101928728 Gene

collagen alpha-1(III) chain-like

LOC101928120 Gene

collagen alpha-1(I) chain-like

COL3A1 Gene

collagen, type III, alpha 1

This gene encodes the pro-alpha1 chains of type III collagen, a fibrillar collagen that is found in extensible connective tissues such as skin, lung, uterus, intestine and the vascular system, frequently in association with type I collagen. Mutations in this gene are associated with Ehlers-Danlos syndrome type IV, and with aortic and arterial aneurysms. [provided by R. Dalgleish, Feb 2008]

COL24A1 Gene

collagen, type XXIV, alpha 1

This gene is a member of the collagen gene family and is thought to regulate type I collagen fibrillogenesis during fetal development. [provided by RefSeq, Mar 2017]

LOC105375110 Gene

collagen alpha-1(III) chain-like

LOC105371184 Gene

collagen alpha-1(I) chain-like

LOC124903828 Gene

collagen alpha-5(IV) chain-like

LOC124905135 Gene

collagen alpha-1(III) chain-like

collagen disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease collagen disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

collagen disease Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores

genes associated with the disease collagen disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

collagen disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease collagen disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

collagen disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease collagen disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Collagen disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Collagen disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Collagen disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Collagen disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Collagen-Vascular Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Collagen-Vascular Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Disseminated Eosinophilic Collagen Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Disseminated Eosinophilic Collagen Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Disseminated eosinophilic collagen disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Disseminated eosinophilic collagen disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

coronary artery disease; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; graves disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease; hypothyroidism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colitis; crohn disease; crohn's disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; graft vs host disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; graft vs host disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

transmembrane collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the transmembrane collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type iv trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type iv trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

fibrillar collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the fibrillar collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type xvi trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type xvi trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type viii trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type viii trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

anchoring collagen complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the anchoring collagen complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type xiii trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type xiii trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

basement membrane collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the basement membrane collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

sheet-forming collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the sheet-forming collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

network-forming collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the network-forming collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type xi trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type xi trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

short-chain collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the short-chain collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type v trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type v trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type iii trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type iii trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type ii trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type ii trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type ix trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type ix trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type vii trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type vii trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type vi trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type vi trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

facit collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the facit collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type xv trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type xv trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type xii trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type xii trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type xiv trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type xiv trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

collagen type i trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the collagen type i trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

transmembrane collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the transmembrane collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type iv trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type iv trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type xviii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type xviii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

network-forming collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the network-forming collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

fibrillar collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the fibrillar collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type xvi trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type xvi trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type viii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type viii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type x trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type x trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type xvii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type xvii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

basement membrane collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the basement membrane collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

sheet-forming collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the sheet-forming collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

anchoring collagen complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the anchoring collagen complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type xi trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type xi trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

short-chain collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the short-chain collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type v trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type v trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type iii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type iii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type ii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type ii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type xii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type xii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type ix trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type ix trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type vii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type vii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type vi trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type vi trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type xiii trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type xiii trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

facit collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the facit collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type xv trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type xv trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type xiv trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type xiv trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen type i trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen type i trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term collagen in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

collagen-activated tyrosine kinase receptor signaling pathway Gene Set

From GO Biological Process Annotations 2015

genes participating in the collagen-activated tyrosine kinase receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of collagen binding Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of collagen binding biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

collagen catabolic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the collagen catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

collagen metabolic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the collagen metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of collagen catabolic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of collagen catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of collagen binding Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of collagen binding biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of collagen binding Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of collagen binding biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of collagen catabolic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of collagen catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.

collagen-activated signaling pathway Gene Set

From GO Biological Process Annotations 2015

genes participating in the collagen-activated signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.

collagen fibril organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the collagen fibril organization biological process from the curated GO Biological Process Annotations 2015 dataset.

collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset.

transmembrane collagen trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the transmembrane collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type iv trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type iv trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type viii trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type viii trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

network-forming collagen trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the network-forming collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

fibrillar collagen trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the fibrillar collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type xvi trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type xvi trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type xiii trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type xiii trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

basement membrane collagen trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the basement membrane collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

sheet-forming collagen trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the sheet-forming collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

anchoring collagen complex Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the anchoring collagen complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type xi trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type xi trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

short-chain collagen trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the short-chain collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type v trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type v trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type iii trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type iii trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type ii trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type ii trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type xv trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type xv trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type xii trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type xii trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type ix trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type ix trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type vii trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type vii trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type vi trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type vi trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

facit collagen trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the facit collagen trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type xiv trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type xiv trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen type i trimer Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the collagen type i trimer cellular component from the curated GO Cellular Component Annotations 2015 dataset.

collagen receptor activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the collagen receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

collagen binding involved in cell-matrix adhesion Gene Set

From GO Molecular Function Annotations 2015

genes performing the collagen binding involved in cell-matrix adhesion molecular function from the curated GO Molecular Function Annotations 2015 dataset.

collagen binding Gene Set

From GO Molecular Function Annotations 2015

genes performing the collagen binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

collagen v binding Gene Set

From GO Molecular Function Annotations 2015

genes performing the collagen v binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

protein tyrosine kinase collagen receptor activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the protein tyrosine kinase collagen receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

impaired collagen-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired collagen-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

type 1 collagen overmodification Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 collagen overmodification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone collagen fibril morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cartilage collagen Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal cartilage collagen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Fibrillar collagen, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fibrillar collagen, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fibronectin, type II, collagen-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fibronectin, type II, collagen-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Collagen alpha-1(XVIII) chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Collagen alpha-1(XVIII) chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Collagen triple helix repeat Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Collagen triple helix repeat protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Collagen IV, non-collagenous Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Collagen IV, non-collagenous protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Collagen alpha-1(XXV) chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Collagen alpha-1(XXV) chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Domain of unknown function DUF959, collagen XVIII, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Domain of unknown function DUF959, collagen XVIII, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased collagen deposition in the muscles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased collagen deposition in the muscles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pulmonary collagen fibril morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pulmonary collagen fibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tendon collagen fibril morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tendon collagen fibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal collagen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal collagen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased collagen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased collagen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal aorta collagen fibril morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal aorta collagen fibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone collagen fibril morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone collagen fibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal dermis reticular layer collagen network Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal dermis reticular layer collagen network phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cutaneous collagen fibril morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cutaneous collagen fibril morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

collagen Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term collagen in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Platelet Adhesion to exposed collagen Gene Set

From Reactome Pathways 2014

proteins participating in the Platelet Adhesion to exposed collagen pathway from the Reactome Pathways dataset.

Crosslinking of collagen fibrils Gene Set

From Reactome Pathways 2014

proteins participating in the Crosslinking of collagen fibrils pathway from the Reactome Pathways dataset.

Assembly of collagen fibrils and other multimeric structures Gene Set

From Reactome Pathways 2014

proteins participating in the Assembly of collagen fibrils and other multimeric structures pathway from the Reactome Pathways dataset.

Collagen formation Gene Set

From Reactome Pathways 2014

proteins participating in the Collagen formation pathway from the Reactome Pathways dataset.

Collagen degradation Gene Set

From Reactome Pathways 2014

proteins participating in the Collagen degradation pathway from the Reactome Pathways dataset.

Collagen biosynthesis and modifying enzymes Gene Set

From Reactome Pathways 2014

proteins participating in the Collagen biosynthesis and modifying enzymes pathway from the Reactome Pathways dataset.

Collagen Nevus Of Skin Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Collagen Nevus Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Cartilage Collagen Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormal Cartilage Collagen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Type Ii Collagen Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormal Type Ii Collagen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Low Grade Fibromyxoid Sarcoma With Giant Collagen Rosettes Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Low Grade Fibromyxoid Sarcoma With Giant Collagen Rosettes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Impaired Collagen-Induced Platelet Aggregation Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Impaired Collagen-Induced Platelet Aggregation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Reduced Muscle Collagen Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Reduced Muscle Collagen in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Collagen Overmodification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Collagen Overmodification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

collagen fibril organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the collagen fibril organization biological process from the curated GO Biological Process Annotations 2023 dataset.

collagen-activated signaling pathway Gene Set

From GO Biological Process Annotations 2023

genes participating in the collagen-activated signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of collagen fibril organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of collagen fibril organization biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of collagen fibril organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of collagen fibril organization biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of collagen catabolic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of collagen catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of collagen catabolic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of collagen catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.

collagen-activated tyrosine kinase receptor signaling pathway Gene Set

From GO Biological Process Annotations 2023

genes participating in the collagen-activated tyrosine kinase receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of collagen fibril organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of collagen fibril organization biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of collagen binding Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of collagen binding biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of collagen catabolic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of collagen catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of collagen binding Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of collagen binding biological process from the curated GO Biological Process Annotations 2023 dataset.

collagen-containing extracellular matrix Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen-containing extracellular matrix cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type I trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type I trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type XI trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type XI trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type II trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type II trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type III trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type III trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type IV trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type IV trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type V trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type V trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type IX trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type IX trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type VIII trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type VIII trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type XV trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type XV trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type VII trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type VII trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type X trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type X trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type XIV trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type XIV trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type XVI trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type XVI trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type XIII trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type XIII trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type XII trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type XII trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

sheet-forming collagen trimer Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the sheet-forming collagen trimer cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen type VII anchoring fibril Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the collagen type VII anchoring fibril cellular component from the curated GO Cellular Component Annotations 2023 dataset.

collagen binding involved in cell-matrix adhesion Gene Set

From GO Molecular Function Annotations 2023

genes performing the collagen binding involved in cell-matrix adhesion molecular function from the curated GO Molecular Function Annotations 2023 dataset.

collagen V binding Gene Set

From GO Molecular Function Annotations 2023

genes performing the collagen V binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

collagen receptor activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the collagen receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

protein tyrosine kinase collagen receptor activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the protein tyrosine kinase collagen receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

abnormal cutaneous collagen fibril morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal cutaneous collagen fibril morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased collagen deposition in the muscles Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased collagen deposition in the muscles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal tendon collagen fibril morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal tendon collagen fibril morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased circulating type I collagen C-terminal telopeptide level Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased circulating type I collagen C-terminal telopeptide level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased circulating type I collagen C-terminal telopeptide level Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased circulating type I collagen C-terminal telopeptide level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal bone collagen fibril morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal bone collagen fibril morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal dermis reticular layer collagen network Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal dermis reticular layer collagen network phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased collagen level Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased collagen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal corneal stroma collagen fibril morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal corneal stroma collagen fibril morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal pulmonary collagen fibril morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal pulmonary collagen fibril morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal aorta collagen fibril morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal aorta collagen fibril morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased collagen level Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased collagen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal collagen level Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal collagen level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Type I collagen synthesis in the context of osteogenesis imperfecta Gene Set

From WikiPathways Pathways 2024

proteins participating in the Type I collagen synthesis in the context of osteogenesis imperfecta pathway from the WikiPathways Pathways 2024 dataset.

Assembly of collagen fibrils and other multimeric structures Gene Set

From Reactome Pathways 2024

proteins participating in the Assembly of collagen fibrils and other multimeric structures pathway from the Reactome Pathways 2024 dataset.

Collagen biosynthesis and modifying enzymes Gene Set

From Reactome Pathways 2024

proteins participating in the Collagen biosynthesis and modifying enzymes pathway from the Reactome Pathways 2024 dataset.

Collagen chain trimerization Gene Set

From Reactome Pathways 2024

proteins participating in the Collagen chain trimerization pathway from the Reactome Pathways 2024 dataset.

Collagen degradation Gene Set

From Reactome Pathways 2024

proteins participating in the Collagen degradation pathway from the Reactome Pathways 2024 dataset.

Collagen formation Gene Set

From Reactome Pathways 2024

proteins participating in the Collagen formation pathway from the Reactome Pathways 2024 dataset.

Crosslinking of collagen fibrils Gene Set

From Reactome Pathways 2024

proteins participating in the Crosslinking of collagen fibrils pathway from the Reactome Pathways 2024 dataset.

Defective VWF binding to collagen type I Gene Set

From Reactome Pathways 2024

proteins participating in the Defective VWF binding to collagen type I pathway from the Reactome Pathways 2024 dataset.

Defects of platelet adhesion to exposed collagen Gene Set

From Reactome Pathways 2024

proteins participating in the Defects of platelet adhesion to exposed collagen pathway from the Reactome Pathways 2024 dataset.

Enhanced binding of GP1BA variant to VWF multimer:collagen Gene Set

From Reactome Pathways 2024

proteins participating in the Enhanced binding of GP1BA variant to VWF multimer:collagen pathway from the Reactome Pathways 2024 dataset.

Platelet Adhesion to exposed collagen Gene Set

From Reactome Pathways 2024

proteins participating in the Platelet Adhesion to exposed collagen pathway from the Reactome Pathways 2024 dataset.

collagen fibril organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the collagen fibril organization biological process from the curated GO Biological Process Annotations 2025 dataset.

collagen catabolic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the collagen catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.

collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.

collagen-activated signaling pathway Gene Set

From GO Biological Process Annotations 2025

genes participating in the collagen-activated signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of collagen fibril organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of collagen fibril organization biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of collagen fibril organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of collagen fibril organization biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of collagen catabolic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of collagen catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of collagen catabolic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of collagen catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.

collagen-activated tyrosine kinase receptor signaling pathway Gene Set

From GO Biological Process Annotations 2025

genes participating in the collagen-activated tyrosine kinase receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of collagen fibril organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of collagen fibril organization biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of collagen binding Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of collagen binding biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of collagen catabolic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of collagen catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of collagen biosynthetic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of collagen biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of collagen metabolic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of collagen metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset.

collagen-containing extracellular matrix Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen-containing extracellular matrix cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type I trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type I trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type II trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type II trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type XI trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type XI trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type III trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type III trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type IV trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type IV trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type V trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type V trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type IX trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type IX trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type VIII trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type VIII trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type X trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type X trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type XIV trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type XIV trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type XVI trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type XVI trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type XIII trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type XIII trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen type XII trimer Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the collagen type XII trimer cellular component from the curated GO Cellular Component Annotations 2025 dataset.

interstitial hexagonal collagen network Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the interstitial hexagonal collagen network cellular component from the curated GO Cellular Component Annotations 2025 dataset.

collagen binding involved in cell-matrix adhesion Gene Set

From GO Molecular Function Annotations 2025

genes performing the collagen binding involved in cell-matrix adhesion molecular function from the curated GO Molecular Function Annotations 2025 dataset.

collagen V binding Gene Set

From GO Molecular Function Annotations 2025

genes performing the collagen V binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

collagen receptor activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the collagen receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

protein tyrosine kinase collagen receptor activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the protein tyrosine kinase collagen receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

Multiple epiphyseal dysplasia due to collagen 9 anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia due to collagen 9 anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

collagen-containing extracellular matrix Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the collagen-containing extracellular matrix cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type VI trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type VI trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen beaded filament Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen beaded filament cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type XIII trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type XIII trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Transmembrane collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Transmembrane collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type I trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type I trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Fibrillar collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Fibrillar collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Banded collagen fibril Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Banded collagen fibril cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Complex of collagen trimers Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Complex of collagen trimers cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type XI trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type XI trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Basement membrane collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Basement membrane collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type XV trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type XV trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type V trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type V trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

FACIT collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the FACIT collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type XIV trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type XIV trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Anchoring collagen complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Anchoring collagen complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type IV trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type IV trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen network Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen network cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

network-forming collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the network-forming collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type III trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type III trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type XII trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type XII trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type XXVI trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type XXVI trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type IX trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type IX trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type VII anchoring fibril Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type VII anchoring fibril cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen anchoring fibril Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen anchoring fibril cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type VII trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type VII trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen sheet Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen sheet cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

sheet-forming collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the sheet-forming collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

short-chain collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the short-chain collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type VIII trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type VIII trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type II trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type II trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type XVI trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type XVI trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Collagen type X trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Collagen type X trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

collagen-containing extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the collagen-containing extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen network Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen network cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Complex of collagen trimers Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Complex of collagen trimers cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen beaded filament Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen beaded filament cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Anchoring collagen complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Anchoring collagen complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Transmembrane collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Transmembrane collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Banded collagen fibril Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Banded collagen fibril cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Fibrillar collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Fibrillar collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type XI trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type XI trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen sheet Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen sheet cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

network-forming collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the network-forming collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type IV trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type IV trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Basement membrane collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Basement membrane collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type VI trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type VI trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type V trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type V trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

short-chain collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the short-chain collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen anchoring fibril Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen anchoring fibril cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type I trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type I trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

sheet-forming collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the sheet-forming collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Medial layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Medial layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type VII anchoring fibril Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type VII anchoring fibril cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type IX trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type IX trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type II trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type II trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type III trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type III trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

FACIT collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the FACIT collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen type XIII trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Collagen type XIII trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Collagen 6-related myopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Collagen 6-related myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

COLLAGEN POLYMORPH Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the COLLAGEN POLYMORPH phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Qualitative or quantitative defects of collagen Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Qualitative or quantitative defects of collagen phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Collagen biosynthesis and extracellular matrix organization Gene Set

From CM4AI U2OS Cell Map Protein Localization Assemblies

proteins comprising Collagen biosynthesis and extracellular matrix organization assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.

Collagen biosynthesis Gene Set

From CM4AI U2OS Cell Map Protein Localization Assemblies

proteins comprising Collagen biosynthesis assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.

Liver fibrosis (total hepatic collagen content) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Liver fibrosis (total hepatic collagen content) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Serum type 1 collagen metabolite levels Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Serum type 1 collagen metabolite levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Platelet reactivity measurement (collagen-ADP) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Platelet reactivity measurement (collagen-ADP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Platelet reactivity measurement (collagen-epinephrine) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Platelet reactivity measurement (collagen-epinephrine) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

crohn disease; crohn's disease; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral arterial disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease; hyperthyroidism; hypothyroidism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease; hyperthyroidism; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; granuloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; granuloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; familial mediterranean fever Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

liver disease; wilson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease liver disease; wilson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; dna damage; genomic instability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; dna damage; genomic instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hemochromatosis; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease ; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease ; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; duodenal diseases; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; sarcoidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison's disease; graves' disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison's disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney disease; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; olfaction disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; autoimmune diseases; graves disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; mercury poisoning, nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; mercury poisoning, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; neurodegenerative diseases; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; neurodegenerative diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; colitis, ulcerative; crohn disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease celiac disease; colitis, ulcerative; crohn disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult-onset still disease; still's disease, adult-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amnesia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amnesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; coronary disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; coronary disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular disease; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular disease; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gaucher disease; nervous system diseases; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; nervous system diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; metabolic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft-versus-host disease; psoriasis; celiac disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft-versus-host disease; psoriasis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease parkinson's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; peripheral vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angina pectoris; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angina pectoris; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; spondylitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; spondylitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; gastrointestinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gaucher disease; legg-perthes disease; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn's disease; ulcerative colitis; inflammatory bowel disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn's disease; ulcerative colitis; inflammatory bowel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; postoperative complications; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular disease; periodontal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular disease; periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary disease; coronary heart disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; dyslipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; disease susceptibility; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; disease susceptibility; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; addison's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; ileal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; ileal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; coronary artery disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; coronary artery disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadaver; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadaver; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

common variable immunodeficiency; crohn disease; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease common variable immunodeficiency; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; arteriosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; dilatation, pathologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; dilatation, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lewy body disease; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lewy body disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyloidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sanhoff disease; tay-sachs disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sanhoff disease; tay-sachs disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; postoperative complications; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; delirium; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; delirium; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease/coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease/coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; hallucinations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; growth disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; lewy body disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; lewy body disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease; myocardial infarction; stroke; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; addison's disease; autoimmune diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; colitis, ulcerative; crohn disease; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease celiac disease; colitis, ulcerative; crohn disease; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; chronic obstructive pulmonary disease/copd Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroid disease; thyroid disease, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroid disease; thyroid disease, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; neural tube defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; cutaneous fistula; rectal fistula Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; cutaneous fistula; rectal fistula in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; spondylarthropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; spondylarthropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Crohn's disease and celiac disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Cardiovascular Disease+Pulmonary Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cardiovascular Disease+Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Parkinson's disease or first degree relation to individual with Parkinson's disease Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Parkinson's disease or first degree relation to individual with Parkinson's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Alzheimer's disease or family history of Alzheimer's disease Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Alzheimer's disease or family history of Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Crohn's disease and celiac disease Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors Gene Set

From Biocarta Pathways

proteins participating in the inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors pathway from the Biocarta Pathways dataset.

deregulation of cdk5 in alzheimers disease Gene Set

From Biocarta Pathways

proteins participating in the deregulation of cdk5 in alzheimers disease pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

Parkinson disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature coronary artery disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature coronary artery disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jakob-Creutzfeldt disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jakob-Creutzfeldt disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher's disease, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher's disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stargardt Disease 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stargardt Disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Norum disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Norum disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Salla disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Salla disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Worth disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Worth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ménière's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ménière's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acute neuronopathic Gaucher's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IVF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IVF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type IXa1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type IXa1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive hypophosphatemic bone disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory bowel disease 25, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory bowel disease 25, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Moyamoya disease 6 with achalasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Moyamoya disease 6 with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IV, congenital neuromuscular Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 4B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 4B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brain small vessel disease with hemorrhage Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

RRM2B-related mitochondrial disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Phytanic acid storage disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Phytanic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 20, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasemia with bone disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasemia with bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented nodular adrenocortical disease, primary, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented nodular adrenocortical disease, primary, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pigmented nodular adrenocortical disease, primary, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chylomicron retention disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chylomicron retention disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Basal ganglia disease, biotin-responsive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Basal ganglia disease, biotin-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coronary artery disease, autosomal dominant 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coronary artery disease, autosomal dominant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hepatic venoocclusive disease with immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hepatic venoocclusive disease with immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Triglyceride storage disease with ichthyosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cowden disease 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cowden disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cowden disease 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cowden disease 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type II, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2A1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IF Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type ID Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IC Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IB Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type IA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schindler disease, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schindler disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schindler disease, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schindler disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-pick disease, intermediate, protracted neurovisceral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-pick disease, intermediate, protracted neurovisceral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 6, autosomal recessive early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudo von Willebrand disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, juvenile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, juvenile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Darier disease, segmental Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Darier disease, segmental phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Naxos disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Naxos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2r Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, axonal, type 2q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leiner disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leiner disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dowling-degos disease 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dowling-degos disease 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, atypical, due to saposin C deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor II deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease 0, muscle Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease 0, muscle phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Subacute neuronopathic Gaucher's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Subacute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lafora disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lafora disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease, type B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease, type A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease, type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type X Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type X phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tangier disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tangier disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cole disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cole disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 8, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 8, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IXa2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IXa2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Refsum disease, adult, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Refsum disease, adult, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart disease, multiple types, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Werdnig-Hoffmann disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Werdnig-Hoffmann disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 19, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 19, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease type C2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Niemann-Pick disease type C1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Niemann-Pick disease type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cholestanol storage disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cholestanol storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cowden disease 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cowden disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-sachs disease, juvenile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-sachs disease, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIa Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stargardt disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stargardt disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor IX deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaucher disease, perinatal lethal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaucher disease, perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alexander's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alexander's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal arthrogryposis with anterior horn cell disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dowling-Degos disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dowling-Degos disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-Sachs disease, B1 variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-Sachs disease, B1 variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mast cell disease, systemic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mast cell disease, systemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease dominant intermediate 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease dominant intermediate 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neutral lipid storage disease with myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, infantile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor XI deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maple syrup urine disease type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maple syrup urine disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease XV Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease XV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemoglobin H disease, nondeletional Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemoglobin H disease, nondeletional phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IXb Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IXb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IXc Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IXc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscle eye brain disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Addison's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Addison's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital cystic disease of liver Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lhermitte-Duclos disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lhermitte-Duclos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kugelberg-Welander disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kugelberg-Welander disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Darier disease, acral hemorrhagic type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Darier disease, acral hemorrhagic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wilson's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wilson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate d Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate d phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate c Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate c phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, recessive intermediate A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, recessive intermediate A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIc Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IIIb Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IIIb phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease ganglioneuroblastoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease ganglioneuroblastoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oguchi's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oguchi's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kanzaki disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kanzaki disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic valve disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic valve disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intermediate maple syrup urine disease type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intermediate maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fish-eye disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sandhoff disease, chronic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sandhoff disease, chronic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, infantile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Central core disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary factor VIII deficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-Sachs disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-Sachs disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease, type 2M Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease, type 2M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tay-Sachs disease, variant AB Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tay-Sachs disease, variant AB phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sialic acid storage disease, severe infantile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2K Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

I cell disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the I cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune disease, multisystem, infantile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the GLYCOGEN STORAGE DISEASE II, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Medullary cystic kidney disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Medullary cystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Danon disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Danon disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dent disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dent disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dent disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dent disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IXd Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IXd phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease, type V Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease, type V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune disease, syndromic multisystem Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune disease, syndromic multisystem phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 2P Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 2P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dent Disease 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dent Disease 2 from the curated CTD Gene-Disease Associations dataset.

Pick Disease of the Brain Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pick Disease of the Brain from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 10 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 12 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 13 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 14 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 15 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 18 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 18 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 19 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 19 from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset.

Parkinson disease 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson disease 9 from the curated CTD Gene-Disease Associations dataset.

Oguchi disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oguchi disease from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease from the curated CTD Gene-Disease Associations dataset.

Tay-Sachs Disease, AB Variant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tay-Sachs Disease, AB Variant from the curated CTD Gene-Disease Associations dataset.

Naxos disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Naxos disease from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2K from the curated CTD Gene-Disease Associations dataset.

Carbamoyl-Phosphate Synthase I Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carbamoyl-Phosphate Synthase I Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

Chylomicron retention disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chylomicron retention disease from the curated CTD Gene-Disease Associations dataset.

Cholesterol Ester Storage Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholesterol Ester Storage Disease from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 6 from the curated CTD Gene-Disease Associations dataset.

Addison Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Addison Disease from the curated CTD Gene-Disease Associations dataset.

Alexander Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alexander Disease from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 16 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 17 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 7 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 4 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease 0, Liver Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease 0, Liver from the curated CTD Gene-Disease Associations dataset.

Tangier Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tangier Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1C from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 26 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 26 from the curated CTD Gene-Disease Associations dataset.

Pigmented Nodular Adrenocortical Disease, Primary, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 1 from the curated CTD Gene-Disease Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate D from the curated CTD Gene-Disease Associations dataset.

Hartnup Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hartnup Disease from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1D from the curated CTD Gene-Disease Associations dataset.

Intervertebral disc disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intervertebral disc disease from the curated CTD Gene-Disease Associations dataset.

Von Willebrand disease, platelet type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Von Willebrand disease, platelet type from the curated CTD Gene-Disease Associations dataset.

Coronary Artery Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Artery Disease from the curated CTD Gene-Disease Associations dataset.

Machado-Joseph Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Machado-Joseph Disease from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease from the curated CTD Gene-Disease Associations dataset.

Papillon-Lefevre Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Papillon-Lefevre Disease from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Moyamoya Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Moyamoya Disease from the curated CTD Gene-Disease Associations dataset.

Gilbert Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gilbert Disease from the curated CTD Gene-Disease Associations dataset.

Congenital thrombotic disease, due to Protein C deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.

Pulmonary Disease, Chronic Obstructive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pulmonary Disease, Chronic Obstructive from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 14 from the curated CTD Gene-Disease Associations dataset.

Coronary Artery Disease, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 9 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 11 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 16 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 12 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 10 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2a1 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease 0, Muscle Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease 0, Muscle from the curated CTD Gene-Disease Associations dataset.

Basal ganglia disease, biotin-responsive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Basal ganglia disease, biotin-responsive from the curated CTD Gene-Disease Associations dataset.

Non-alcoholic Fatty Liver Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Non-alcoholic Fatty Liver Disease from the curated CTD Gene-Disease Associations dataset.

Graves Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Graves Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2A2 from the curated CTD Gene-Disease Associations dataset.

Hepatic Veno-Occlusive Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatic Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset.

Hepatic venoocclusive disease with immunodeficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatic venoocclusive disease with immunodeficiency from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 25, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 25, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative from the curated CTD Gene-Disease Associations dataset.

Stargardt disease 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stargardt disease 3 from the curated CTD Gene-Disease Associations dataset.

Stargardt disease 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stargardt disease 4 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type IV Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type IV from the curated CTD Gene-Disease Associations dataset.

Refsum Disease, Infantile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Refsum Disease, Infantile from the curated CTD Gene-Disease Associations dataset.

Polycystic liver disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic liver disease from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 8, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 8, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

Celiac Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Celiac Disease from the curated CTD Gene-Disease Associations dataset.

Genetic Predisposition to Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Genetic Predisposition to Disease from the curated CTD Gene-Disease Associations dataset.

Dimauro disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dimauro disease from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease IXB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease IXB from the curated CTD Gene-Disease Associations dataset.

Coronary Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Disease from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease, Secondary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease, Secondary from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Demyelinating, Type 1e from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Type 4j Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4j from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate A from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

GALLBLADDER DISEASE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GALLBLADDER DISEASE 1 from the curated CTD Gene-Disease Associations dataset.

Acute Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acute Disease from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 3, Autosomal Dominant Lewy Body Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 3, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset.

Brain Small Vessel Disease with Hemorrhage Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset.

Ornithine Carbamoyltransferase Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ornithine Carbamoyltransferase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease, Type IXD Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease, Type IXD from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 5, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 5, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

GLYCOGEN STORAGE DISEASE IXa1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE IXa1 from the curated CTD Gene-Disease Associations dataset.

Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease XII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease XII from the curated CTD Gene-Disease Associations dataset.

Legionnaires' Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Legionnaires' Disease from the curated CTD Gene-Disease Associations dataset.

Hepatorenal form of glycogen storage disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hepatorenal form of glycogen storage disease from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.

Schindler Disease, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Schindler Disease, Type I from the curated CTD Gene-Disease Associations dataset.

Pulmonary Veno-Occlusive Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pulmonary Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4A from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset.

Huntington Disease-Like 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease-Like 3 from the curated CTD Gene-Disease Associations dataset.

Refsum Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Refsum Disease from the curated CTD Gene-Disease Associations dataset.

Aland Island Eye Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aland Island Eye Disease from the curated CTD Gene-Disease Associations dataset.

Bowen's Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bowen's Disease from the curated CTD Gene-Disease Associations dataset.

Hodgkin Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hodgkin Disease from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II from the curated CTD Gene-Disease Associations dataset.

Niemann-Pick Disease, Type C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Niemann-Pick Disease, Type C from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate C from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 2 from the curated CTD Gene-Disease Associations dataset.

Pyruvate Dehydrogenase Complex Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyruvate Dehydrogenase Complex Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 13 from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L from the curated CTD Gene-Disease Associations dataset.

Medullary Cystic Kidney Disease 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Medullary Cystic Kidney Disease 2 from the curated CTD Gene-Disease Associations dataset.

von Willebrand Disease, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease von Willebrand Disease, Type 3 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4C from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 4E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4E from the curated CTD Gene-Disease Associations dataset.

Huntington Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Huntington Disease from the curated CTD Gene-Disease Associations dataset.

PAGET DISEASE, JUVENILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PAGET DISEASE, JUVENILE from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE, LATE-ONSET Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE, LATE-ONSET from the curated CTD Gene-Disease Associations dataset.

Neutral Lipid Storage Disease with Myopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutral Lipid Storage Disease with Myopathy from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type III from the curated CTD Gene-Disease Associations dataset.

End Stage Liver Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease End Stage Liver Disease from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type II from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 5 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Recessive Intermediate A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Recessive Intermediate A from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 6 from the curated CTD Gene-Disease Associations dataset.

Hashimoto Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hashimoto Disease from the curated CTD Gene-Disease Associations dataset.

Canavan Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Canavan Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1F from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2G from the curated CTD Gene-Disease Associations dataset.

Krabbe Disease, Atypical, due to Saposin A Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset.

Stargardt disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Stargardt disease 1 from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease XIII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease XIII from the curated CTD Gene-Disease Associations dataset.

Lafora Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lafora Disease from the curated CTD Gene-Disease Associations dataset.

Van Buchem disease type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Van Buchem disease type 2 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Disease Models, Animal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Disease Models, Animal from the curated CTD Gene-Disease Associations dataset.

Fabry Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fabry Disease from the curated CTD Gene-Disease Associations dataset.

Motor Neuron Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Motor Neuron Disease from the curated CTD Gene-Disease Associations dataset.

Niemann-Pick Disease, Type A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Niemann-Pick Disease, Type A from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type VII Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type VII from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 3 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 5 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 8 from the curated CTD Gene-Disease Associations dataset.

dowling-degos disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease dowling-degos disease from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 6, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 6, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset.

Darier Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Darier Disease from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease from the curated CTD Gene-Disease Associations dataset.

Paget Disease Of Bone 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paget Disease Of Bone 4 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2D from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2E from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2I from the curated CTD Gene-Disease Associations dataset.

Disease Progression Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Disease Progression from the curated CTD Gene-Disease Associations dataset.

Disease Susceptibility Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Disease Susceptibility from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B from the curated CTD Gene-Disease Associations dataset.

Dent Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dent Disease from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2F from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2J from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, Type 2H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2H from the curated CTD Gene-Disease Associations dataset.

Lewy Body Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lewy Body Disease from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 16 from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 12 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Axonal, Type 2n Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2n from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 1, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

De Vivo disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease De Vivo disease from the curated CTD Gene-Disease Associations dataset.

Alzheimer disease type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer disease type 4 from the curated CTD Gene-Disease Associations dataset.

Alzheimer disease type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer disease type 2 from the curated CTD Gene-Disease Associations dataset.

Leigh Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leigh Disease from the curated CTD Gene-Disease Associations dataset.

Pigmented Nodular Adrenocortical Disease, Primary, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 2 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 28, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 28, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Dominant Intermediate B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate B from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease IXC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease IXC from the curated CTD Gene-Disease Associations dataset.

Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset.

AORTIC VALVE DISEASE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AORTIC VALVE DISEASE 1 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type VI Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type VI from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease IB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease IB from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 10 from the curated CTD Gene-Disease Associations dataset.

Niemann-Pick Disease, Type B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Niemann-Pick Disease, Type B from the curated CTD Gene-Disease Associations dataset.

Raynaud Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Raynaud Disease from the curated CTD Gene-Disease Associations dataset.

Moyamoya disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Moyamoya disease 1 from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease Type IIb Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease Type IIb from the curated CTD Gene-Disease Associations dataset.

Moyamoya disease 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Moyamoya disease 3 from the curated CTD Gene-Disease Associations dataset.

Niemann-Pick disease, type C2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Niemann-Pick disease, type C2 from the curated CTD Gene-Disease Associations dataset.

Hodgkin disease, X-linked pseudoautosomal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hodgkin disease, X-linked pseudoautosomal from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 8 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 9 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 7 from the curated CTD Gene-Disease Associations dataset.

Sialic Acid Storage Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sialic Acid Storage Disease from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 24 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 24 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease from the curated CTD Gene-Disease Associations dataset.

Gallbladder Disease 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gallbladder Disease 4 from the curated CTD Gene-Disease Associations dataset.

Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 20 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 22 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 22 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 27 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 27 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth Disease, Type 4H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4H from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 21 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 21 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 15 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 23 from the curated CTD Gene-Disease Associations dataset.

Charcot-Marie-Tooth disease, X-linked recessive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 2 from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.

GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset.

Peripheral Arterial Occlusive Disease 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Arterial Occlusive Disease 1 from the curated CTD Gene-Disease Associations dataset.