Name

MSL3P1 Gene

male-specific lethal 3 homolog (Drosophila) pseudogene 1

Predicted to be involved in chromatin organization and regulation of DNA-templated transcription. Predicted to be located in nucleus. Predicted to be part of MSL complex and NuA4 histone acetyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025]

LLGL2 Gene

lethal giant larvae homolog 2 (Drosophila)

The lethal (2) giant larvae protein of Drosophila plays a role in asymmetric cell division, epithelial cell polarity, and cell migration. This human gene encodes a protein similar to lethal (2) giant larvae of Drosophila. In fly, the protein's ability to localize cell fate determinants is regulated by the atypical protein kinase C (aPKC). In human, this protein interacts with aPKC-containing complexes and is cortically localized in mitotic cells. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

LLGL1 Gene

lethal giant larvae homolog 1 (Drosophila)

This gene encodes a protein that is similar to a tumor suppressor in Drosophila. The protein is part of a cytoskeletal network and is associated with nonmuscle myosin II heavy chain and a kinase that specifically phosphorylates this protein at serine residues. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]

MSL2 Gene

male-specific lethal 2 homolog (Drosophila)

Enables histone H2B ubiquitin ligase activity. Involved in DNA damage response and protein monoubiquitination. Part of MSL complex and nucleus. Is active in chromatin. [provided by Alliance of Genome Resources, Mar 2025]

MSL3 Gene

male-specific lethal 3 homolog (Drosophila)

This gene encodes a nuclear protein that is similar to the product of the Drosophila male-specific lethal-3 gene. The Drosophila protein plays a critical role in a dosage-compensation pathway, which equalizes X-linked gene expression in males and females. Thus, the human protein is thought to play a similar function in chromatin remodeling and transcriptional regulation, and it has been found as part of a complex that is responsible for histone H4 lysine-16 acetylation. This gene can undergo X inactivation. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2, 7 and 8. [provided by RefSeq, Jul 2010]

MSL1 Gene

male-specific lethal 1 homolog (Drosophila)

Enables protein-macromolecule adaptor activity. Involved in positive regulation of DNA-templated transcription. Located in nucleoplasm. Part of MSL complex. [provided by Alliance of Genome Resources, Mar 2025]

LOC100499192 Gene

male-specific lethal 3 homolog (Drosophila) pseudogene

LOC100499191 Gene

male-specific lethal 3 homolog (Drosophila) pseudogene

CASQ1 Gene

calsequestrin 1 (fast-twitch, skeletal muscle)

This gene encodes the skeletal muscle specific member of the calsequestrin protein family. Calsequestrin functions as a luminal sarcoplasmic reticulum calcium sensor in both cardiac and skeletal muscle cells. This protein, also known as calmitine, functions as a calcium regulator in the mitochondria of skeletal muscle. This protein is absent in patients with Duchenne and Becker types of muscular dystrophy. [provided by RefSeq, Jun 2013]

TNNT1 Gene

troponin T type 1 (skeletal, slow)

This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

GEM Gene

GTP binding protein overexpressed in skeletal muscle

The protein encoded by this gene belongs to the RAD/GEM family of GTP-binding proteins. It is associated with the inner face of the plasma membrane and could play a role as a regulatory protein in receptor-mediated signal transduction. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]

MYL3 Gene

myosin, light chain 3, alkali; ventricular, skeletal, slow

MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]

MYL1 Gene

myosin, light chain 1, alkali; skeletal, fast

Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain expressed in fast skeletal muscle. Two transcript variants have been identified for this gene. [provided by RefSeq, Jul 2008]

MUSK Gene

muscle, skeletal, receptor tyrosine kinase

This gene encodes a muscle-specific tyrosine kinase receptor. The encoded protein may play a role in clustering of the acetylcholine receptor in the postsynaptic neuromuscular junction. Mutations in this gene have been associated with congenital myasthenic syndrome. Alternatively spliced transcript variants have been described.[provided by RefSeq, Oct 2009]

USMG5 Gene

up-regulated during skeletal muscle growth 5 homolog (mouse)

Predicted to be involved in proton motive force-driven ATP synthesis. Located in mitochondrion. Part of proton-transporting ATP synthase complex. Implicated in mitochondrial complex V (ATP synthase) deficiency nuclear type 6. [provided by Alliance of Genome Resources, Mar 2025]

TNNT3 Gene

troponin T type 3 (skeletal, fast)

The binding of Ca(2+) to the trimeric troponin complex initiates the process of muscle contraction. Increased Ca(2+) concentrations produce a conformational change in the troponin complex that is transmitted to tropomyosin dimers situated along actin filaments. The altered conformation permits increased interaction between a myosin head and an actin filament which, ultimately, produces a muscle contraction. The troponin complex has protein subunits C, I, and T. Subunit C binds Ca(2+) and subunit I binds to actin and inhibits actin-myosin interaction. Subunit T binds the troponin complex to the tropomyosin complex and is also required for Ca(2+)-mediated activation of actomyosin ATPase activity. There are 3 different troponin T genes that encode tissue-specific isoforms of subunit T for fast skeletal-, slow skeletal-, and cardiac-muscle. This gene encodes fast skeletal troponin T protein; also known as troponin T type 3. Alternative splicing results in multiple transcript variants encoding additional distinct troponin T type 3 isoforms. A developmentally regulated switch between fetal/neonatal and adult troponin T type 3 isoforms occurs. Additional splice variants have been described but their biological validity has not been established. Mutations in this gene may cause distal arthrogryposis multiplex congenita type 2B (DA2B). [provided by RefSeq, Oct 2009]

TNNI2 Gene

troponin I type 2 (skeletal, fast)

This gene encodes a fast-twitch skeletal muscle protein, a member of the troponin I gene family, and a component of the troponin complex including troponin T, troponin C and troponin I subunits. The troponin complex, along with tropomyosin, is responsible for the calcium-dependent regulation of striated muscle contraction. Mouse studies show that this component is also present in vascular smooth muscle and may play a role in regulation of smooth muscle function. In addition to muscle tissues, this protein is found in corneal epithelium, cartilage where it is an inhibitor of angiogenesis to inhibit tumor growth and metastasis, and mammary gland where it functions as a co-activator of estrogen receptor-related receptor alpha. This protein also suppresses tumor growth in human ovarian carcinoma. Mutations in this gene cause myopathy and distal arthrogryposis type 2B. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]

TNNI1 Gene

troponin I type 1 (skeletal, slow)

Troponin proteins associate with tropomyosin and regulate the calcium sensitivity of the myofibril contractile apparatus of striated muscles. Troponin I (TnI), along with troponin T (TnT) and troponin C (TnC), is one of 3 subunits that form the troponin complex of the thin filaments of striated muscle. TnI is the inhibitory subunit; blocking actin-myosin interactions and thereby mediating striated muscle relaxation. The TnI subfamily contains three genes: TnI-skeletal-fast-twitch, TnI-skeletal-slow-twitch, and TnI-cardiac. The TnI-fast and TnI-slow genes are expressed in fast-twitch and slow-twitch skeletal muscle fibers, respectively, while the TnI-cardiac gene is expressed exclusively in cardiac muscle tissue. This gene encodes the Troponin-I-skeletal-slow-twitch protein. This gene is expressed in cardiac and skeletal muscle during early development but is restricted to slow-twitch skeletal muscle fibers in adults. The encoded protein prevents muscle contraction by inhibiting calcium-mediated conformational changes in actin-myosin complexes. [provided by RefSeq, Jul 2008]

MYLPF Gene

myosin light chain, phosphorylatable, fast skeletal muscle

Predicted to enable calcium ion binding activity. Predicted to be a structural constituent of muscle. Involved in muscle contraction. Located in lysosomal membrane. Implicated in distal arthrogryposis type 1C. [provided by Alliance of Genome Resources, Mar 2025]

RYR1 Gene

ryanodine receptor 1 (skeletal)

This gene encodes a ryanodine receptor found in skeletal muscle. The encoded protein functions as a calcium release channel in the sarcoplasmic reticulum but also serves to connect the sarcoplasmic reticulum and transverse tubule. Mutations in this gene are associated with malignant hyperthermia susceptibility, central core disease, and minicore myopathy with external ophthalmoplegia. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

ACTA1 Gene

actin, alpha 1, skeletal muscle

The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause a variety of myopathies, including nemaline myopathy, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects with manifestations such as hypotonia. [provided by RefSeq, Sep 2019]

MYH13 Gene

myosin, heavy chain 13, skeletal muscle

Predicted to enable actin filament binding activity and microfilament motor activity. Predicted to be involved in muscle contraction. Predicted to act upstream of or within cellular response to starvation. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025]

MRSD Gene

mental retardation-skeletal dysplasia

MYH2 Gene

myosin, heavy chain 2, skeletal muscle, adult

Myosins are actin-based motor proteins that function in the generation of mechanical force in eukaryotic cells. Muscle myosins are heterohexamers composed of 2 myosin heavy chains and 2 pairs of nonidentical myosin light chains. This gene encodes a member of the class II or conventional myosin heavy chains, and functions in skeletal muscle contraction. This gene is found in a cluster of myosin heavy chain genes on chromosome 17. A mutation in this gene results in inclusion body myopathy-3. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2009]

MYH3 Gene

myosin, heavy chain 3, skeletal muscle, embryonic

Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome. [provided by RefSeq, Jul 2008]

MYH1 Gene

myosin, heavy chain 1, skeletal muscle, adult

Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. Myosin heavy chains are encoded by a multigene family. In mammals at least 10 different myosin heavy chain (MYH) isoforms have been described from striated, smooth, and nonmuscle cells. These isoforms show expression that is spatially and temporally regulated during development. [provided by RefSeq, Jul 2008]

MYH4 Gene

myosin, heavy chain 4, skeletal muscle

Enables double-stranded RNA binding activity. Involved in muscle contraction. Located in myofibril. [provided by Alliance of Genome Resources, Mar 2025]

MYH8 Gene

myosin, heavy chain 8, skeletal muscle, perinatal

Myosins are actin-based motor proteins that function in the generation of mechanical force in eukaryotic cells. Muscle myosins are heterohexamers composed of 2 myosin heavy chains and 2 pairs of nonidentical myosin light chains. This gene encodes a member of the class II or conventional myosin heavy chains, and functions in skeletal muscle contraction. This gene is predominantly expressed in fetal skeletal muscle. This gene is found in a cluster of myosin heavy chain genes on chromosome 17. A mutation in this gene results in trismus-pseudocamptodactyly syndrome. [provided by RefSeq, Sep 2009]

lethal skeletal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the lethal skeletal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Lethal Skeletal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Lethal skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Platyspondylic Lethal Skeletal Dysplasia, Torrance Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Platyspondylic Lethal Skeletal Dysplasia, Torrance Type from the curated CTD Gene-Disease Associations dataset.

Platyspondylic Lethal Skeletal Dysplasia, Torrance Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Platyspondylic Lethal Skeletal Dysplasia, Torrance Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal short-limb skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal short-limb skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal occipital encephalocele-skeletal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal occipital encephalocele-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

NEK9-related lethal skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the NEK9-related lethal skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal osteosclerotic bone dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal osteosclerotic bone dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

skeletal muscle satellite cell maintenance involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle satellite cell maintenance involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.

Eiken Skeletal Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Eiken Skeletal Dysplasia from the curated CTD Gene-Disease Associations dataset.

skeletal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the skeletal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

craniofacial-skeletal-dermatologic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial-skeletal-dermatologic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

greenberg skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the greenberg skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

platyspondylic skeletal dysplasia, torrance type Gene Set

From OMIM Gene-Disease Associations

genes associated with the platyspondylic skeletal dysplasia, torrance type phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation-skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation-skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

Skeletal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Skeletal Dysplasia With Acanthosis Nigricans Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Skeletal Dysplasia With Acanthosis Nigricans in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Eiken Skeletal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Craniofacial-skeletal-dermatologic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Craniofacial-skeletal-dermatologic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Skeletal dysplasia and progressive central nervous system degeneration Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Skeletal dysplasia and progressive central nervous system degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

COL2A1-related skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the COL2A1-related skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Lethal multiple pterygium syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteogenesis imperfecta, recessive perinatal lethal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteogenesis imperfecta, recessive perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contracture syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amish lethal microcephaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amish lethal microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Popliteal pterygium syndrome lethal type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Popliteal pterygium syndrome lethal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contractural syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contractural syndrome 3 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.

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.

Lethal congenital contracture syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa, lethal acantholytic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa, lethal acantholytic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Clostridium difficile lethal toxin B Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Clostridium difficile lethal toxin B from the curated CTD Gene-Chemical Interactions dataset.

Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal from the curated CTD Gene-Disease Associations dataset.

Tight skin contracture syndrome, lethal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tight skin contracture syndrome, lethal from the curated CTD Gene-Disease Associations dataset.

Lethal Congenital Contracture Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Congenital Contracture Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset.

Finnish lethal neonatal metabolic syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Finnish lethal neonatal metabolic syndrome from the curated CTD Gene-Disease Associations dataset.

Amish lethal microcephaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amish lethal microcephaly from the curated CTD Gene-Disease Associations dataset.

Lethal congenital contracture syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal congenital contracture syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Lethal Congenital Contractural Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Congenital Contractural Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Epidermolysis bullosa, lethal acantholytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis bullosa, lethal acantholytic from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease of Heart, Lethal Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.

Gaucher Disease, Perinatal Lethal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaucher Disease, Perinatal Lethal from the curated CTD Gene-Disease Associations dataset.

Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease from the curated CTD Gene-Disease Associations dataset.

lethal midline granuloma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

lethal Gene Set

From GeneRIF Biological Term Annotations

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

lethal short-limbed short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the lethal short-limbed short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Granuloma, Lethal Midline Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Granuloma, Lethal Midline phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lethal giant larvae (Lgl)-like, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lethal giant larvae (Lgl)-like, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lethal(2) giant larvae protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lethal(2) giant larvae protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lethal giant larvae homologue 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lethal giant larvae homologue 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein male-specific lethal-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein male-specific lethal-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset.

popliteal pterygium syndrome 2, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the popliteal pterygium syndrome 2, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple pterygium syndrome, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From OMIM Gene-Disease Associations

genes associated with the rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.

arthrogryposis, lethal, with anterior horn cell disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the arthrogryposis, lethal, with anterior horn cell disease phenotype from the curated OMIM Gene-Disease Associations dataset.

epidermolysis bullosa, lethal acantholytic Gene Set

From OMIM Gene-Disease Associations

genes associated with the epidermolysis bullosa, lethal acantholytic phenotype from the curated OMIM Gene-Disease Associations dataset.

glycogen storage disease of heart, lethal congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the glycogen storage disease of heart, lethal congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

gaucher disease, perinatal lethal Gene Set

From OMIM Gene-Disease Associations

genes associated with the gaucher disease, perinatal lethal phenotype from the curated OMIM Gene-Disease Associations dataset.

restrictive dermopathy, lethal Gene Set

From OMIM Gene-Disease Associations

genes associated with the restrictive dermopathy, lethal phenotype from the curated OMIM Gene-Disease Associations dataset.

cpt ii deficiency, lethal neonatal Gene Set

From OMIM Gene-Disease Associations

genes associated with the cpt ii deficiency, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contractural syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contractural syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contractural syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contractural syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Lethal Congenital Contractural Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Congenital Contractural Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Rigidity And Multifocal Seizure Syndrome, Lethal Neonatal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Pterygium Syndrome, Lethal Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Pterygium Syndrome, Lethal Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Congenital Contracture Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Congenital Contracture Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Short-Limbed Short Stature Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Short-Limbed Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Tight Skin Contracture Syndrome (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Tight Skin Contracture Syndrome (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Gaucher Disease, Perinatal Lethal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Gaucher Disease, Perinatal Lethal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Osteochondrodysplasia, Complex Lethal, Symoens-Barnes-Gistelinck Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Osteochondrodysplasia, Complex Lethal, Symoens-Barnes-Gistelinck Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lethal midline granuloma Gene Set

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

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

Lethal congenital contracture syndrome Gene Set

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

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

Lethal congenital glycogen storage disease of heart Gene Set

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

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

Lethal congenital contracture syndrome 2 Gene Set

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

genes co-occuring with the disease Lethal congenital contracture syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal congenital contracture syndrome 1 Gene Set

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

genes co-occuring with the disease Lethal congenital contracture syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal congenital contracture syndrome 3 Gene Set

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

genes co-occuring with the disease Lethal congenital contracture syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Gaucher's disease perinatal lethal Gene Set

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

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

Lethal congenital contracture syndrome 4 Gene Set

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

genes co-occuring with the disease Lethal congenital contracture syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lethal tight skin contracture syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal tight skin contracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Gaucher disease perinatal lethal Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Gaucher disease perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal congenital contracture syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal congenital contracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal arthrogryposis-anterior horn cell disease syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal arthrogryposis-anterior horn cell disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal congenital contractural syndrome Finnish Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal congenital contractural syndrome Finnish phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal congenital glycogen storage disease of heart Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal congenital glycogen storage disease of heart phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Perinatal lethal hypophosphatasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Perinatal lethal hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal acantholytic epidermolysis bullosa Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal acantholytic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal multiple pterygium syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Amish lethal microcephaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Amish lethal microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal Kniest-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal Kniest-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal Encephalopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal Encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal polymalformative syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal polymalformative syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Complex lethal osteochondrodysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Complex lethal osteochondrodysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

skeletal muscle hypertrophy is regulated via akt-mtor pathway Gene Set

From Biocarta Pathways

proteins participating in the skeletal muscle hypertrophy is regulated via akt-mtor pathway pathway from the Biocarta Pathways dataset.

Cerebro-oculo-facio-skeletal syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebro-oculo-facio-skeletal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen content in skeletal muscle, increased Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen content in skeletal muscle, increased phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal muscle sarcoglycan complex SGC, beta-gamma-delta-zeta Gene Set

From CORUM Protein Complexes

proteins in the Skeletal muscle sarcoglycan complex SGC, beta-gamma-delta-zeta protein complex from the CORUM Protein Complexes dataset.

Skeletal muscle sarcoglycan complex SGC, epsilon-beta-gamma-delta Gene Set

From CORUM Protein Complexes

proteins in the Skeletal muscle sarcoglycan complex SGC, epsilon-beta-gamma-delta protein complex from the CORUM Protein Complexes dataset.

Dystrophin-sarcoglycan-syntrophin complex, skeletal muscle Gene Set

From CORUM Protein Complexes

proteins in the Dystrophin-sarcoglycan-syntrophin complex, skeletal muscle protein complex from the CORUM Protein Complexes dataset.

Nitric oxide synthase-dystrophin complex, skeletal muscle Gene Set

From CORUM Protein Complexes

proteins in the Nitric oxide synthase-dystrophin complex, skeletal muscle protein complex from the CORUM Protein Complexes dataset.

Skeletal muscle sarcoglycan complex SGC, alpha-beta-gamma-delta Gene Set

From CORUM Protein Complexes

proteins in the Skeletal muscle sarcoglycan complex SGC, alpha-beta-gamma-delta protein complex from the CORUM Protein Complexes dataset.

Skeletal muscle sarcoglycan complex SGC, alpha-beta-epsilon-gamma Gene Set

From CORUM Protein Complexes

proteins in the Skeletal muscle sarcoglycan complex SGC, alpha-beta-epsilon-gamma protein complex from the CORUM Protein Complexes dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

skeletal tuberculosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

skeletal muscle cancer Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

diffuse idiopathic skeletal hyperostosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

skeletal muscle neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

skeletal frame size Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skeletal frame size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

age-related skeletal disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age-related skeletal disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skeletal responsiveness to estrogen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skeletal responsiveness to estrogen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

axial skeletal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease axial skeletal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skeletal muscle properties Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skeletal muscle properties in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skeletal hyperostosis Gene Set

From GAD Gene-Disease Associations

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

skeletal Gene Set

From GeneRIF Biological Term Annotations

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

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Dermatomyositis_Muscle - Striated (Skeletal) (MMHCC)_GSE1551 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Dermatomyositis_Muscle - Striated (Skeletal) (MMHCC)_GSE1551 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

COPD - Chronic obstructive pulmonary disease_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE475 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during COPD - Chronic obstructive pulmonary disease_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE475 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Obesity_Muscle - Striated (Skeletal) (MMHCC)_GSE474 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Obesity_Muscle - Striated (Skeletal) (MMHCC)_GSE474 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Type 1 diabetes mellitus_Muscle - Striated (Skeletal) (MMHCC)_GSE1659 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Type 1 diabetes mellitus_Muscle - Striated (Skeletal) (MMHCC)_GSE1659 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Obesity_Muscle - Striated (Skeletal) (MMHCC)_GSE5109 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Obesity_Muscle - Striated (Skeletal) (MMHCC)_GSE5109 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Dermatomyositis_Muscle - Striated (Skeletal) (MMHCC)_GSE5370 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Dermatomyositis_Muscle - Striated (Skeletal) (MMHCC)_GSE5370 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

YY1_Deficiency_GDS4856_318_mouse_Soleus skeletal muscle Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the YY1_Deficiency_GDS4856_318_mouse_Soleus skeletal muscle gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

MSTN_DEPLETION_GDS3637_94_mouse_mature skeletal muscle Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the MSTN_DEPLETION_GDS3637_94_mouse_mature skeletal muscle gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

LAMA2_Deficiency_GDS3371_595_mouse_Hind limb skeletal muscle (4-week old dy3K/dy3K animals) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the LAMA2_Deficiency_GDS3371_595_mouse_Hind limb skeletal muscle (4-week old dy3K/dy3K animals) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

TP53INP2_OE_GDS5054_276_mouse_SKM-Tg - Skeletal muscle Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TP53INP2_OE_GDS5054_276_mouse_SKM-Tg - Skeletal muscle gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

DES_KO_GDS4804_171_mouse_young skeletal muscles Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the DES_KO_GDS4804_171_mouse_young skeletal muscles gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.

embryonic skeletal joint morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the embryonic skeletal joint morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle atrophy Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle thin filament assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle thin filament assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle adaptation Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle adaptation biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle organ development Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle organ development biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of satellite cell activation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

branchiomeric skeletal muscle development Gene Set

From GO Biological Process Annotations 2015

genes participating in the branchiomeric skeletal muscle development biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle hypertrophy Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle hypertrophy biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle satellite cell differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle satellite cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle contraction via regulation of action potential Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle contraction via regulation of action potential biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle fiber adaptation Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle fiber adaptation biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle adaptation Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle adaptation biological process from the curated GO Biological Process Annotations 2015 dataset.

twitch skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the twitch skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

growth factor dependent regulation of skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the growth factor dependent regulation of skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

voluntary skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the voluntary skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of satellite cell activation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal system morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal system morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

slow-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.

extraocular skeletal muscle development Gene Set

From GO Biological Process Annotations 2015

genes participating in the extraocular skeletal muscle development biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal myofibril assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal myofibril assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle satellite cell commitment Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle satellite cell commitment biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal system development Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal system development biological process from the curated GO Biological Process Annotations 2015 dataset.

embryonic skeletal system development Gene Set

From GO Biological Process Annotations 2015

genes participating in the embryonic skeletal system development biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle satellite cell migration Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle satellite cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of fast-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of fast-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

involuntary skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the involuntary skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

embryonic skeletal limb joint morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the embryonic skeletal limb joint morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

relaxation of skeletal muscle Gene Set

From GO Biological Process Annotations 2015

genes participating in the relaxation of skeletal muscle biological process from the curated GO Biological Process Annotations 2015 dataset.

embryonic skeletal joint development Gene Set

From GO Biological Process Annotations 2015

genes participating in the embryonic skeletal joint development biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of fast-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of fast-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

myoblast differentiation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the myoblast differentiation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of twitch skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of twitch skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset.

myoblast migration involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the myoblast migration involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of skeletal muscle contraction by calcium ion signaling Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of skeletal muscle contraction by calcium ion signaling biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle satellite cell activation Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle satellite cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.

embryonic skeletal system morphogenesis Gene Set

From GO Biological Process Annotations 2015

genes participating in the embryonic skeletal system morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

skeletal muscle myosin thick filament assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

myotube differentiation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2015

genes participating in the myotube differentiation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.

abnormality of the skeletal system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skeletal morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

neoplasm of the skeletal system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the neoplasm of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

skeletal muscle Gene Set

From HPA Tissue Gene Expression Profiles

genes with high or low expression in skeletal muscle relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.

skeletal muscle Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in skeletal muscle relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

skeletal muscle atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the skeletal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the skeletal system Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the skeletal system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skeletal morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skeletal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fatty replacement of skeletal muscle Gene Set

From HPO Gene-Disease Associations

genes associated with the fatty replacement of skeletal muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skeletal maturation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skeletal maturation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skeletal myopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the skeletal myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the skeletal system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the skeletal system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skeletal muscle fiber size Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skeletal muscle fiber size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skeletal muscle hypertrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the skeletal muscle hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

accelerated skeletal maturation Gene Set

From HPO Gene-Disease Associations

genes associated with the accelerated skeletal maturation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the skeletal musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the skeletal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

centrally nucleated skeletal muscle fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the centrally nucleated skeletal muscle fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skeletal physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skeletal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

delayed skeletal maturation Gene Set

From HPO Gene-Disease Associations

genes associated with the delayed skeletal maturation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple skeletal anomalies Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple skeletal anomalies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hyperostosis, Diffuse Idiopathic Skeletal Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hyperostosis, Diffuse Idiopathic Skeletal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Troponin T, fast skeletal muscle Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Troponin T, fast skeletal muscle protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cattle cerebrum and skeletal muscle-specific protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cattle cerebrum and skeletal muscle-specific protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

skeletal muscle fiber atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle fiber morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle fiber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle fiber density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle fiber density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal muscle fiber number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal muscle weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle hypertrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent skeletal muscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent skeletal muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle mechanoreceptor morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle mechanoreceptor morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle fiber diameter Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle fiber diameter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal tumor incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal muscle glycogen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle fiber triad morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle fiber triad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle fiber necrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle fiber necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired skeletal muscle contractility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired skeletal muscle contractility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle fiber number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle interstitial fibrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle interstitial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle fiber size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle fiber size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased variability of skeletal muscle fiber size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased variability of skeletal muscle fiber size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired skeletal muscle regeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired skeletal muscle regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle fibrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle necrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal muscle fiber size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle fiber size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle satellite cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle satellite cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal muscle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal muscle mass Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle fiber degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle fiber degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

centrally nucleated skeletal muscle fibers Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the centrally nucleated skeletal muscle fibers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased skeletal muscle fiber diameter Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased skeletal muscle fiber diameter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle glycogen level Gene Set

From MPO Gene-Phenotype Associations

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

skeletal muscle hypotrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle hypotrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle regeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle fiber size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle fiber size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle endomysial fibrosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal skeletal muscle fiber type ratio Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal skeletal muscle fiber type ratio phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Gene Set

From Reactome Pathways 2014

proteins participating in the Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) pathway from the Reactome Pathways dataset.

Skeletal Muscle Male Gene Set

From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles

genes with high or low DNA methylation in Skeletal Muscle Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.

Skeletal Muscle Female Gene Set

From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles

genes with high or low DNA methylation in Skeletal Muscle Female relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.

skeletal muscle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue skeletal muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

skeletal system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue skeletal system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

skeletal muscle cancer cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue skeletal muscle cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

skeletal muscle cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue skeletal muscle cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

skeletal system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue skeletal system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

skeletal muscle Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue skeletal muscle in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

skeletal muscle cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue skeletal muscle cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

skeletal muscle cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue skeletal muscle cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

skeletal muscle fiber Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue skeletal muscle fiber in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

skeletal muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue skeletal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

skeletal system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue skeletal system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

skeletal muscle cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue skeletal muscle cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Muscle-skeletal muscle satellite stem cell Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Muscle-skeletal muscle satellite stem cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Skin-cell of skeletal muscle Gene Set

From Tabula Sapiens Gene-Cell Associations

genes with high or low expression in Skin-cell of skeletal muscle relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.

Abnormality Of The Skeletal System Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormality Of The Skeletal System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Skeletal Malformation Gene Set

From DisGeNET Gene-Disease Associations

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

Neoplasm Of Skeletal System Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neoplasm Of Skeletal System in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Autoimmune Inflammation Of Skeletal Muscle Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Autoimmune Inflammation Of Skeletal Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Skeletal Muscle Steatosis Gene Set

From DisGeNET Gene-Disease Associations

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

Skeletal Malocclusion Gene Set

From DisGeNET Gene-Disease Associations

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

Radiohumeral Fusions With Other Skeletal And Craniofacial Anomalies Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Radiohumeral Fusions With Other Skeletal And Craniofacial Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Skeletal Muscle Neoplasm Gene Set

From DisGeNET Gene-Disease Associations

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

Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Swelling Of Skeletal Muscle Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Swelling Of Skeletal Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Other Congenital Malformation Syndromes With Other Skeletal Changes Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Other Congenital Malformation Syndromes With Other Skeletal Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Accessory Skeletal Muscle Gene Set

From DisGeNET Gene-Disease Associations

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

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Skeletal Muscle Atrophy Gene Set

From DisGeNET Gene-Phenotype Associations

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

Abnormality Of Skeletal Morphology Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of Skeletal Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Centrally Nucleated Skeletal Muscle Fibers Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Centrally Nucleated Skeletal Muscle Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormality Of Skeletal Muscle Fiber Size Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of Skeletal Muscle Fiber Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Skeletal Muscle Hypertrophy Gene Set

From DisGeNET Gene-Phenotype Associations

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

Fatty Replacement Of Skeletal Muscle Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Fatty Replacement Of Skeletal Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Internally Nucleated Skeletal Muscle Fibers Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Internally Nucleated Skeletal Muscle Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Skeletal Anomalies Gene Set

From DisGeNET Gene-Phenotype Associations

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

Aplasia/Hypoplasia Involving The Skeletal Musculature Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Aplasia/Hypoplasia Involving The Skeletal Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Fasciculation, Skeletal Muscle Gene Set

From DisGeNET Gene-Phenotype Associations

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

Skeletal Muscle Tender Gene Set

From DisGeNET Gene-Phenotype Associations

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

Skeletal Muscle Fibrosis Gene Set

From DisGeNET Gene-Phenotype Associations

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

Fatigable Weakness Of Skeletal Muscles Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Fatigable Weakness Of Skeletal Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Glycogen Content In Skeletal Muscle, Increased Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Glycogen Content In Skeletal Muscle, Increased in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormality Of Skeletal Maturation Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of Skeletal Maturation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Skeletal Muscle Paralysis Gene Set

From DisGeNET Gene-Phenotype Associations

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

myoblast fusion involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the myoblast fusion involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle organ development Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle organ development biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal system development Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal system development biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle hypertrophy Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle hypertrophy biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of the force of skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of the force of skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

relaxation of skeletal muscle Gene Set

From GO Biological Process Annotations 2023

genes participating in the relaxation of skeletal muscle biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2023 dataset.

myoblast migration involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the myoblast migration involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.

embryonic skeletal joint development Gene Set

From GO Biological Process Annotations 2023

genes participating in the embryonic skeletal joint development biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of fast-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of fast-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal system morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal system morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle thin filament assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle thin filament assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle myosin thick filament assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle atrophy Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal myofibril assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal myofibril assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

branchiomeric skeletal muscle development Gene Set

From GO Biological Process Annotations 2023

genes participating in the branchiomeric skeletal muscle development biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of satellite cell activation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

embryonic skeletal system development Gene Set

From GO Biological Process Annotations 2023

genes participating in the embryonic skeletal system development biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2023 dataset.

embryonic skeletal joint morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the embryonic skeletal joint morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle satellite cell migration Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle satellite cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.

growth factor dependent regulation of skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the growth factor dependent regulation of skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of slow-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2023 dataset.

embryonic skeletal system morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the embryonic skeletal system morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

embryonic skeletal limb joint morphogenesis Gene Set

From GO Biological Process Annotations 2023

genes participating in the embryonic skeletal limb joint morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle contraction by action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle contraction by action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

extraocular skeletal muscle development Gene Set

From GO Biological Process Annotations 2023

genes participating in the extraocular skeletal muscle development biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle contraction via regulation of action potential Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle contraction via regulation of action potential biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle adaptation Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle adaptation biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

myotube cell development involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the myotube cell development involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

myotube differentiation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the myotube differentiation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle satellite cell differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle satellite cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle hypertrophy Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle hypertrophy biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2023 dataset.

slow-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

fast-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the fast-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle contraction by calcium ion signaling Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle contraction by calcium ion signaling biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle hypertrophy Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle hypertrophy biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle contraction by chemo-mechanical energy conversion Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle contraction by chemo-mechanical energy conversion biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of fast-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of fast-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle adaptation Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle adaptation biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of satellite cell activation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of twitch skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of twitch skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

involuntary skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the involuntary skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.

twitch skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2023

genes participating in the twitch skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2023 dataset.

abnormal skeletal muscle morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal skeletal muscle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle hypertrophy Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle hypertrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal skeletal muscle fiber morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal skeletal muscle fiber morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle hypotrophy Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle hypotrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal muscle fiber size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased skeletal muscle fiber size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

impaired skeletal muscle regeneration Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the impaired skeletal muscle regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased skeletal muscle mass Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased skeletal muscle mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased skeletal muscle fiber density Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased skeletal muscle fiber density phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle hypoplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

centrally nucleated skeletal muscle fibers Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the centrally nucleated skeletal muscle fibers phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal skeletal muscle satellite cell proliferation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal skeletal muscle satellite cell proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

delayed skeletal muscle regeneration Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the delayed skeletal muscle regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased skeletal muscle fiber diameter Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased skeletal muscle fiber diameter phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased skeletal muscle glycogen level Gene Set

From MGI Mouse Phenotype Associations 2023

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

impaired skeletal muscle contractility Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the impaired skeletal muscle contractility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased skeletal muscle fiber number Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased skeletal muscle fiber number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal skeletal muscle fiber type ratio Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal skeletal muscle fiber type ratio phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle fiber atrophy Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle atrophy Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased variability of skeletal muscle fiber size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased variability of skeletal muscle fiber size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle interstitial fibrosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle interstitial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle fiber necrosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle fiber necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle necrosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal muscle mass Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased skeletal muscle mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal muscle fiber diameter Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased skeletal muscle fiber diameter phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle endomysial fibrosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle endomysial fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent skeletal muscle Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent skeletal muscle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle fiber degeneration Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle fiber degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle fibrosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle degeneration Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

enhanced skeletal muscle regeneration Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the enhanced skeletal muscle regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased skeletal muscle fiber size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased skeletal muscle fiber size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal muscle glycogen level Gene Set

From MGI Mouse Phenotype Associations 2023

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

decreased skeletal muscle triglyceride level Gene Set

From MGI Mouse Phenotype Associations 2023

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

abnormal skeletal muscle triglyceride level Gene Set

From MGI Mouse Phenotype Associations 2023

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

abnormal skeletal muscle fiber triad morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal skeletal muscle fiber triad morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased skeletal muscle weight Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased skeletal muscle weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal skeletal muscle regeneration Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal skeletal muscle regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal muscle fiber number Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased skeletal muscle fiber number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

skeletal muscle hyperplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the skeletal muscle hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal muscle size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased skeletal muscle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal muscle triglyceride level Gene Set

From MGI Mouse Phenotype Associations 2023

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

increased skeletal muscle weight Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased skeletal muscle weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased skeletal muscle size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased skeletal muscle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal tumor incidence Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased skeletal tumor incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal skeletal muscle size Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal skeletal muscle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased skeletal muscle cell apoptosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased skeletal muscle cell apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal skeletal muscle mass Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal skeletal muscle mass phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal skeletal muscle morphology Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the abnormal skeletal muscle morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

increased skeletal muscle mass Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the increased skeletal muscle mass phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

decreased skeletal muscle mass Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the decreased skeletal muscle mass phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

Muscle - Skeletal Gene Set

From GTEx Tissue Gene Expression Profiles 2023

genes with high or low expression in Muscle - Skeletal relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.

Human - Fetal Development - L1 - Skeletal muscle cells Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Fetal Development - L1 - Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Fetal Development - L2 - Muscle-Skeletal muscle cells Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Fetal Development - L2 - Muscle-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Human - Fetal Development - L2 - Eye-Skeletal muscle cells Gene Set

From HuBMAP Azimuth Cell Type Annotations

genes associated with the Human - Fetal Development - L2 - Eye-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.

Skeletal muscle precursor cell_Cartilage_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Skeletal muscle precursor cell_Cartilage_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Perichondrial embryonic skeletal stem cell_Bone marrow_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Perichondrial embryonic skeletal stem cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Skeletal stem and progenitor cell (SSPC)_Cartilage_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Skeletal stem and progenitor cell (SSPC)_Cartilage_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Skeletal muscle stem cell_Embryoid body_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Skeletal muscle stem cell_Embryoid body_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Skeletal muscle stem cell_Skeletal muscle_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Skeletal muscle stem cell_Skeletal muscle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Skeletal myoblast_Muscle_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Skeletal myoblast_Muscle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Skeletal muscle cell_Skeletal muscle_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Skeletal muscle cell_Skeletal muscle_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Skeletal muscle cell_Skeletal muscle_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Skeletal muscle cell_Skeletal muscle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Skeletal muscle cell_Skin_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Skeletal muscle cell_Skin_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

SCFA and skeletal muscle substrate metabolism Gene Set

From WikiPathways Pathways 2024

proteins participating in the SCFA and skeletal muscle substrate metabolism pathway from the WikiPathways Pathways 2024 dataset.

Cholesterol biosynthesis with skeletal dysplasias Gene Set

From WikiPathways Pathways 2024

proteins participating in the Cholesterol biosynthesis with skeletal dysplasias pathway from the WikiPathways Pathways 2024 dataset.

Endochondral ossification with skeletal dysplasias Gene Set

From WikiPathways Pathways 2024

proteins participating in the Endochondral ossification with skeletal dysplasias pathway from the WikiPathways Pathways 2024 dataset.

TGF beta receptor signaling in skeletal dysplasias Gene Set

From WikiPathways Pathways 2024

proteins participating in the TGF beta receptor signaling in skeletal dysplasias pathway from the WikiPathways Pathways 2024 dataset.

Catabolism of skeletal muscle in cachexia Gene Set

From WikiPathways Pathways 2024

proteins participating in the Catabolism of skeletal muscle in cachexia pathway from the WikiPathways Pathways 2024 dataset.

myoblast fusion involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the myoblast fusion involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle organ development Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle organ development biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal system development Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal system development biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle hypertrophy Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle hypertrophy biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of the force of skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of the force of skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

relaxation of skeletal muscle Gene Set

From GO Biological Process Annotations 2025

genes participating in the relaxation of skeletal muscle biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2025 dataset.

myoblast migration involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the myoblast migration involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of skeletal muscle tissue growth Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of skeletal muscle tissue growth biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.

embryonic skeletal joint development Gene Set

From GO Biological Process Annotations 2025

genes participating in the embryonic skeletal joint development biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of fast-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of fast-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal system morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal system morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle thin filament assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle thin filament assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle myosin thick filament assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle myosin thick filament assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle atrophy Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal myofibril assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal myofibril assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

branchiomeric skeletal muscle development Gene Set

From GO Biological Process Annotations 2025

genes participating in the branchiomeric skeletal muscle development biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of satellite cell activation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

embryonic skeletal system development Gene Set

From GO Biological Process Annotations 2025

genes participating in the embryonic skeletal system development biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2025 dataset.

embryonic skeletal joint morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the embryonic skeletal joint morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle satellite cell migration Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle satellite cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.

growth factor dependent regulation of skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the growth factor dependent regulation of skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of slow-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2025 dataset.

embryonic skeletal system morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the embryonic skeletal system morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle satellite cell differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle satellite cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

embryonic skeletal limb joint morphogenesis Gene Set

From GO Biological Process Annotations 2025

genes participating in the embryonic skeletal limb joint morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle contraction by action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle contraction by action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

extraocular skeletal muscle development Gene Set

From GO Biological Process Annotations 2025

genes participating in the extraocular skeletal muscle development biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle contraction via regulation of action potential Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle contraction via regulation of action potential biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle contraction by regulation of release of sequestered calcium ion biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle adaptation Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle adaptation biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle fiber development Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle fiber development biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

myotube cell development involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the myotube cell development involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

myotube differentiation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the myotube differentiation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

myoblast differentiation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the myoblast differentiation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

satellite cell activation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of skeletal muscle cell differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle satellite cell proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle satellite cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle tissue development Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle tissue development biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle hypertrophy Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle hypertrophy biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle satellite cell differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle satellite cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle contraction by calcium ion signaling Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle contraction by calcium ion signaling biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.

slow-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

fast-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the fast-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle hypertrophy Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle hypertrophy biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle contraction by chemo-mechanical energy conversion Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle contraction by chemo-mechanical energy conversion biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of fast-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of fast-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle adaptation Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle adaptation biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of satellite cell activation involved in skeletal muscle regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of skeletal muscle tissue regeneration Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of skeletal muscle tissue regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of twitch skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of twitch skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

involuntary skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the involuntary skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

skeletal muscle cell proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of skeletal muscle fiber differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of skeletal muscle fiber differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.

twitch skeletal muscle contraction Gene Set

From GO Biological Process Annotations 2025

genes participating in the twitch skeletal muscle contraction biological process from the curated GO Biological Process Annotations 2025 dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Skeletal muscle cancer Gene Set

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

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

Diffuse idiopathic skeletal hyperostosis Gene Set

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

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

Skeletal tuberculosis Gene Set

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

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

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

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

genes co-occuring with the disease Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Skeletal muscle neoplasm Gene Set

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

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

Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies Gene Set

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

genes co-occuring with the disease Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2 Gene Set

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

genes co-occuring with the disease Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 Gene Set

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

genes co-occuring with the disease Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Skeletal system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Skeletal system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Skeletal muscle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle cancer cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Skeletal muscle cancer cell from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Skeletal muscle in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Skeletal system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Skeletal system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Skeletal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle fiber Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Skeletal muscle fiber in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Skeletal muscle cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle cancer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Skeletal muscle cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Skeletal muscle cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle satellite cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Skeletal muscle satellite cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle satellite stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Skeletal muscle satellite stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Activated skeletal muscle satellite cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Activated skeletal muscle satellite cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Quiescent skeletal muscle satellite cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Quiescent skeletal muscle satellite cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Proliferating skeletal muscle satellite cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Proliferating skeletal muscle satellite cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Skeletal muscle myofibril Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

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

Hereditary skeletal muscle disorder Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hereditary skeletal muscle disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

MYH7-related skeletal myopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the MYH7-related skeletal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Abnormality of the skeletal system Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Abnormality of the skeletal system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cutaneous-skeletal hypophosphatemia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cutaneous-skeletal hypophosphatemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

RHIZOMELIC SKELETAL DYSPLA Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the RHIZOMELIC SKELETAL DYSPLA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Abnormal skeletal morphology Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Abnormal skeletal morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Congenital heart defects and skeletal malformations syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital heart defects and skeletal malformations syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Skeletal dysplaisia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Skeletal dysplaisia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Skeletal myopathy Gene Set

From ClinVar Gene-Phenotype Associations 2025

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

Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Skeletal muscle index Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Skeletal muscle index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Pediatric areal bone mineral density (concordant skeletal phenotype) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Pediatric areal bone mineral density (concordant skeletal phenotype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Pediatric areal bone mineral density (radius vs spine & hip discordant skeletal phenotype) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Pediatric areal bone mineral density (radius vs spine & hip discordant skeletal phenotype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Frontometaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontometaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Czech dysplasia metatarsal type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Czech dysplasia metatarsal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloperipheral dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloperipheral dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wolcott-Rallison dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wolcott-Rallison dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniodiaphyseal dysplasia, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniodiaphyseal dysplasia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypohidrotic X-linked ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypohidrotic X-linked ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive pseudorheumatoid dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteoglophonic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteoglophonic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gracile bone dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gracile bone dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontonasal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontonasal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaphyseal dysplasia, Kozlowski type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaphyseal dysplasia, Kozlowski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Odontoonychodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Odontoonychodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia with multiple dislocations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia with multiple dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal-hepatic-pancreatic dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal-hepatic-pancreatic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acampomelic campomelic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acampomelic campomelic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia/short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia, Missouri type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia, Missouri type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypohidrotic ectodermal dysplasia with immune deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypohidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofrontonasal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofrontonasal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anhidrotic ectodermal dysplasia with immune deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anhidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia, kimberley type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia, kimberley type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac valvular dysplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trichorhinophalangeal dysplasia type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trichorhinophalangeal dysplasia type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diastrophic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diastrophic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thanatophoric dysplasia type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thanatophoric dysplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive hypohidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cleidocranial dysplasia, forme fruste, with brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cleidocranial dysplasia, forme fruste, with brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniometaphyseal dysplasia, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniometaphyseal dysplasia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schneckenbecken dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schneckenbecken dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acromicric dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acromicric dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Terminal osseous dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Terminal osseous dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vitreoretinopathy with phalangeal epiphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitreoretinopathy with phalangeal epiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acromesomelic dysplasia Maroteaux type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acromesomelic dysplasia Maroteaux type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rapp-Hodgkin ectodermal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rapp-Hodgkin ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schimke immunoosseous dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schimke immunoosseous dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acrocapitofemoral dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acrocapitofemoral dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hay-Wells syndrome of ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hay-Wells syndrome of ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oculodentodigital dysplasia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oculodentodigital dysplasia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Greenberg dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Greenberg dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Boomerang dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Boomerang dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniolenticulosutural dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniolenticulosutural dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oculodentodigital dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oculodentodigital dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Desbuquois dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Desbuquois dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bent bone dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bent bone dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chondroectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chondroectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ischiopatellar dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ischiopatellar dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Geleophysic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Geleophysic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Geleophysic dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Geleophysic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia, Aggrecan type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia, Aggrecan type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alveolar capillary dysplasia with misalignment of pulmonary veins Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brachyrachia (short spine dysplasia) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brachyrachia (short spine dysplasia) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia-focal epilepsy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia Strudwick type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia Strudwick type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Septo-optic dysplasia sequence Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Septo-optic dysplasia sequence phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia Maroteaux type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia Maroteaux type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylo-megaepiphyseal-metaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylo-megaepiphyseal-metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cranioectodermal dysplasia 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cranioectodermal dysplasia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cranioectodermal dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cranioectodermal dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cranioectodermal dysplasia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cranioectodermal dysplasia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cranioectodermal dysplasia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cranioectodermal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrous dysplasia of jaw Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrous dysplasia of jaw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Smith McCort dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Smith McCort dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia congenita Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia congenita phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia skin fragility syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia, pakistani type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia, pakistani type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kniest dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kniest dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Otospondylomegaepiphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Otospondylomegaepiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaepiphyseal dysplasia short limb-hand type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia-syndactyly syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia-syndactyly syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Metatrophic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Metatrophic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontonasal dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontonasal dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontonasal dysplasia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontonasal dysplasia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hidrotic ectodermal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dyssegmental dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dyssegmental dysplasia from the curated CTD Gene-Disease Associations dataset.

Frontometaphyseal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Frontometaphyseal dysplasia from the curated CTD Gene-Disease Associations dataset.

DEVELOPMENTAL DYSPLASIA OF THE HIP 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEVELOPMENTAL DYSPLASIA OF THE HIP 1 from the curated CTD Gene-Disease Associations dataset.

GNATHODIAPHYSEAL DYSPLASIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GNATHODIAPHYSEAL DYSPLASIA from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia 3, Anhidrotic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia 3, Anhidrotic from the curated CTD Gene-Disease Associations dataset.

Acrocapitofemoral Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acrocapitofemoral Dysplasia from the curated CTD Gene-Disease Associations dataset.

Thanatophoric dysplasia, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thanatophoric dysplasia, type 2 from the curated CTD Gene-Disease Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac valvular dysplasia, X-linked from the curated CTD Gene-Disease Associations dataset.

GREENBERG DYSPLASIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GREENBERG DYSPLASIA from the curated CTD Gene-Disease Associations dataset.

Craniolenticulosutural Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniolenticulosutural Dysplasia from the curated CTD Gene-Disease Associations dataset.

Mandibuloacral dysplasia with type B lipodystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mandibuloacral dysplasia with type B lipodystrophy from the curated CTD Gene-Disease Associations dataset.

CRANIOECTODERMAL DYSPLASIA 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CRANIOECTODERMAL DYSPLASIA 2 from the curated CTD Gene-Disease Associations dataset.

ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 from the curated CTD Gene-Disease Associations dataset.

Focal cortical dysplasia of Taylor Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Focal cortical dysplasia of Taylor from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.

Multicystic renal dysplasia, bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multicystic renal dysplasia, bilateral from the curated CTD Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

Cranioectodermal Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cranioectodermal Dysplasia from the curated CTD Gene-Disease Associations dataset.

TERMINAL OSSEOUS DYSPLASIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TERMINAL OSSEOUS DYSPLASIA from the curated CTD Gene-Disease Associations dataset.

Thanatophoric Dysplasia, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thanatophoric Dysplasia, Type I from the curated CTD Gene-Disease Associations dataset.

Acromicric dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acromicric dysplasia from the curated CTD Gene-Disease Associations dataset.

Langer mesomelic dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Langer mesomelic dysplasia from the curated CTD Gene-Disease Associations dataset.

Cleidocranial Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cleidocranial Dysplasia from the curated CTD Gene-Disease Associations dataset.

FRONTONASAL DYSPLASIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FRONTONASAL DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.

FRONTONASAL DYSPLASIA 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FRONTONASAL DYSPLASIA 2 from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Bronchopulmonary Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchopulmonary Dysplasia from the curated CTD Gene-Disease Associations dataset.

Spondylo-Megaepiphyseal-Metaphyseal Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylo-Megaepiphyseal-Metaphyseal Dysplasia from the curated CTD Gene-Disease Associations dataset.

Spondyloepiphyseal Dysplasia Tarda, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepiphyseal Dysplasia Tarda, X-Linked from the curated CTD Gene-Disease Associations dataset.

Polyostotic osteolytic dysplasia, hereditary expansile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyostotic osteolytic dysplasia, hereditary expansile from the curated CTD Gene-Disease Associations dataset.

FRONTONASAL DYSPLASIA 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FRONTONASAL DYSPLASIA 3 from the curated CTD Gene-Disease Associations dataset.

Schimke immunoosseous dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Schimke immunoosseous dysplasia from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia from the curated CTD Gene-Disease Associations dataset.

ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency without anhidrotic ectodermal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency without anhidrotic ectodermal dysplasia from the curated CTD Gene-Disease Associations dataset.

Craniofrontonasal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniofrontonasal dysplasia from the curated CTD Gene-Disease Associations dataset.

Oculodentodigital Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oculodentodigital Dysplasia from the curated CTD Gene-Disease Associations dataset.

Anal sphincter dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anal sphincter dysplasia from the curated CTD Gene-Disease Associations dataset.

Anauxetic dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anauxetic dysplasia from the curated CTD Gene-Disease Associations dataset.

Hypopituitarism and septooptic 'dysplasia' Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset.

Odontoonychodermal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Odontoonychodermal dysplasia from the curated CTD Gene-Disease Associations dataset.

Spondylometaphyseal dysplasia, Kozlowski type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaphyseal dysplasia, Kozlowski type from the curated CTD Gene-Disease Associations dataset.

Cortical Dysplasia-Focal Epilepsy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cortical Dysplasia-Focal Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

SPONDYLOPERIPHERAL DYSPLASIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOPERIPHERAL DYSPLASIA from the curated CTD Gene-Disease Associations dataset.

RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.

Spondyloepiphyseal Dysplasia, Kimberley Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepiphyseal Dysplasia, Kimberley Type from the curated CTD Gene-Disease Associations dataset.

Craniometaphyseal Dysplasia, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniometaphyseal Dysplasia, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Schneckenbecken dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Schneckenbecken dysplasia from the curated CTD Gene-Disease Associations dataset.

Thanatophoric Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thanatophoric Dysplasia from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia/ skin fragility syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia/ skin fragility syndrome from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Ghosal Hematodiaphyseal Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ghosal Hematodiaphyseal Dysplasia from the curated CTD Gene-Disease Associations dataset.

Smith-McCort Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Smith-McCort Dysplasia from the curated CTD Gene-Disease Associations dataset.

Diastrophic dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diastrophic dysplasia from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Fibrous Dysplasia, Polyostotic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrous Dysplasia, Polyostotic from the curated CTD Gene-Disease Associations dataset.

RETINAL DYSPLASIA, PRIMARY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY from the curated CTD Gene-Disease Associations dataset.

SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE from the curated CTD Gene-Disease Associations dataset.

Fibrous Dysplasia of Bone Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrous Dysplasia of Bone from the curated CTD Gene-Disease Associations dataset.

Metaphyseal Dysplasia without Hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metaphyseal Dysplasia without Hypotrichosis from the curated CTD Gene-Disease Associations dataset.

OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA from the curated CTD Gene-Disease Associations dataset.

Boomerang dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Boomerang dysplasia from the curated CTD Gene-Disease Associations dataset.

Pelviscapular dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pelviscapular dysplasia from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.

GELEOPHYSIC DYSPLASIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GELEOPHYSIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.

Torticollis keloids cryptorchidism renal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Torticollis keloids cryptorchidism renal dysplasia from the curated CTD Gene-Disease Associations dataset.

Campomelic Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Campomelic Dysplasia from the curated CTD Gene-Disease Associations dataset.

Alveolar capillary dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alveolar capillary dysplasia from the curated CTD Gene-Disease Associations dataset.

Ischiopatellar dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ischiopatellar dysplasia from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE from the curated CTD Gene-Disease Associations dataset.

Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Renal hepatic pancreatic dysplasia Dandy Walker cyst Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal hepatic pancreatic dysplasia Dandy Walker cyst from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset.

Nail dysplasia, isolated congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nail dysplasia, isolated congenital from the curated CTD Gene-Disease Associations dataset.

ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

DENTIN DYSPLASIA, TYPE II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DENTIN DYSPLASIA, TYPE II from the curated CTD Gene-Disease Associations dataset.

Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.

Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset.

Mandibuloacral dysplasia with type A lipodystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mandibuloacral dysplasia with type A lipodystrophy from the curated CTD Gene-Disease Associations dataset.

Oculodentodigital Dysplasia, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oculodentodigital Dysplasia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Spondyloepimetaphyseal Dysplasia, Missouri Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Missouri Type from the curated CTD Gene-Disease Associations dataset.

SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS from the curated CTD Gene-Disease Associations dataset.

Acromesomelic dysplasia, Maroteaux type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acromesomelic dysplasia, Maroteaux type from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia 1, Anhidrotic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia 1, Anhidrotic from the curated CTD Gene-Disease Associations dataset.

ACROPECTOROVERTEBRAL DYSPLASIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ACROPECTOROVERTEBRAL DYSPLASIA from the curated CTD Gene-Disease Associations dataset.

Spondyloepiphyseal dysplasia, congenita Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepiphyseal dysplasia, congenita from the curated CTD Gene-Disease Associations dataset.

Spondyloepimetaphyseal Dysplasia, Pakistani Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Pakistani Type from the curated CTD Gene-Disease Associations dataset.

Spondyloepimetaphyseal Dysplasia, Aggrecan Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Aggrecan Type from the curated CTD Gene-Disease Associations dataset.

Parietal Foramina With Cleidocranial Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parietal Foramina With Cleidocranial Dysplasia from the curated CTD Gene-Disease Associations dataset.

Kniest dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Kniest dysplasia from the curated CTD Gene-Disease Associations dataset.

SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.

Frontonasal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Frontonasal dysplasia from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia, hypohidrotic, with immune deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia, hypohidrotic, with immune deficiency from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 1 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 3 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 2 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 5 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 4 from the curated CTD Gene-Disease Associations dataset.

Hip Dysplasia, Beukes Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hip Dysplasia, Beukes Type from the curated CTD Gene-Disease Associations dataset.

craniometaphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

thanatophoric dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

campomelic dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

otospondylomegaepiphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

kniest dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

sost-related sclerosing bone dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

boomerang dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

cleidocranial dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

spondyloepiphyseal dysplasia congenita Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia, strudwick type Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease spondyloepimetaphyseal dysplasia, strudwick type from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

diastrophic dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

hypohidrotic ectodermal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

multiple epiphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

thanatophoric dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

metaphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia, strudwick type Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease spondyloepimetaphyseal dysplasia, strudwick type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

dentin dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia, missouri type Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease spondyloepimetaphyseal dysplasia, missouri type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spondyloepiphyseal dysplasia congenita Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia, sponastrime type Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease spondyloepimetaphyseal dysplasia, sponastrime type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple epiphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

acromesomelic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

anauxetic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

craniometaphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

sost-related sclerosing bone dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease sost-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cleidocranial dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

benign mammary dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

acromesomelic dysplasia, maroteaux type Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease acromesomelic dysplasia, maroteaux type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

schneckenbecken dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

otospondylomegaepiphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

craniodiaphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

diastrophic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

thymic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

hypohidrotic ectodermal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

campomelic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

kniest dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

boomerang dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

acrocapitofemoral dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

fibrous dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

achondroplasia; musculoskeletal abnormalities; osteochondrodysplasias; thanatophoric dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease achondroplasia; musculoskeletal abnormalities; osteochondrodysplasias; thanatophoric dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple epiphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; infant, newborn, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibromuscular dysplasia; hypertension; renal artery obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibromuscular dysplasia; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thanatophoric dysplasia Gene Set

From GAD Gene-Disease Associations

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

arrhythmogenic right ventricular dysplasia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intestinal neuronal dysplasia type b (ind b) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal neuronal dysplasia type b (ind b) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia Gene Set

From GAD Gene-Disease Associations

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

bronchopulmonary dysplasia; respiratory distress syndrome, neonatal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; heart failure Gene Set

From GAD Gene-Disease Associations

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

multiple epiphyseal dysplasia; pseudoachondroplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple epiphyseal dysplasia; pseudoachondroplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular cardiomyopathy/dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular cardiomyopathy/dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ectodermal dysplasia; esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ectodermal dysplasia; esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; cardiomyopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; cardiomyopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoarthritis; hip dysplasia Gene Set

From GAD Gene-Disease Associations

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

fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pseudoachondroplasia and multiple epiphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pseudoachondroplasia and multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

strudwick variant of spondyloepimetaphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease strudwick variant of spondyloepimetaphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple oesophageal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple oesophageal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

risk of cervical dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease risk of cervical dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hpv-associated cervical dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hpv-associated cervical dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; chorioamnionitis Gene Set

From GAD Gene-Disease Associations

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

arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autosomal dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autosomal dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleidocranial dysplasia Gene Set

From GAD Gene-Disease Associations

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

familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia. Gene Set

From GAD Gene-Disease Associations

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

bronchopulmonary dysplasia; Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; ectodermal dysplasia; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; ectodermal dysplasia; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrous dysplasia Gene Set

From GAD Gene-Disease Associations

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

dysplasia Gene Set

From GeneRIF Biological Term Annotations

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

Bronchopulmonary dysplasia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bronchopulmonary dysplasia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

nail dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the nail dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

retinal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple epiphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple epiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

acetabular dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the acetabular dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hip dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the hip dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chorioretinal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the chorioretinal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

metaphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the metaphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fibrous dysplasia of the bones Gene Set

From HPO Gene-Disease Associations

genes associated with the fibrous dysplasia of the bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

frontoparietal cortical dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the frontoparietal cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cortical dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

brainstem dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the brainstem dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spondylometaphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the spondylometaphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

polyostotic fibrous dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the polyostotic fibrous dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cystic renal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cystic renal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fingernail dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the fingernail dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

epiphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the epiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ectodermal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic nerve dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the optic nerve dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multicystic kidney dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the multicystic kidney dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypohidrotic ectodermal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the hypohidrotic ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

polycystic kidney dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the polycystic kidney dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hair-nail ectodermal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the hair-nail ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

toenail dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the toenail dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the renal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diaphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the diaphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

septo-optic dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the septo-optic dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dysplasia of the femoral head Gene Set

From HPO Gene-Disease Associations

genes associated with the dysplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Septo-Optic Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Septo-Optic Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bronchopulmonary Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bronchopulmonary Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ectodermal Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ectodermal Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Thanatophoric Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Thanatophoric Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fibromuscular Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fibromuscular Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fibrous Dysplasia, Polyostotic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fibrous Dysplasia, Polyostotic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fibrous Dysplasia of Bone Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fibrous Dysplasia of Bone phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cleidocranial Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cleidocranial Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Uterine Cervical Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Uterine Cervical Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Arrhythmogenic Right Ventricular Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Adrenocortical dysplasia protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adrenocortical dysplasia protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

?corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

?epiphyseal dysplasia, multiple, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epiphyseal dysplasia, multiple, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloperipheral dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloperipheral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

acampomelic campomelic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the acampomelic campomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

frontometaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontometaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

campomelic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the campomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 4 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

developmental dysplasia of the hip 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the developmental dysplasia of the hip 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

smith-mccort dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the smith-mccort dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

parietal foramina with cleidocranial dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the parietal foramina with cleidocranial dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

craniometaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniometaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

renal-hepatic-pancreatic dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal-hepatic-pancreatic dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 6, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 6, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia/short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia/short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 6 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

focal cortical dysplasia, taylor balloon cell type Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal cortical dysplasia, taylor balloon cell type phenotype from the curated OMIM Gene-Disease Associations dataset.

thanatophoric dysplasia, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the thanatophoric dysplasia, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

mandibuloacral dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mandibuloacral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia, ectrodactyly, and macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

diastrophic dysplasia, broad bone-platyspondylic variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the diastrophic dysplasia, broad bone-platyspondylic variant phenotype from the curated OMIM Gene-Disease Associations dataset.

cleft lip/palate-ectodermal dysplasia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleft lip/palate-ectodermal dysplasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

otospondylomegaepiphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the otospondylomegaepiphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

boomerang dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the boomerang dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

frontonasal dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontonasal dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

frontonasal dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontonasal dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

craniolenticulosutural dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniolenticulosutural dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cranioectodermal dysplasia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cranioectodermal dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cranioectodermal dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cranioectodermal dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cranioectodermal dysplasia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cranioectodermal dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cranioectodermal dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cranioectodermal dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 7 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 3, witkop type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 3, witkop type phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaepiphyseal dysplasia, short limb-hand type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 7, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 7, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

oculodentodigital dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculodentodigital dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia, anhidrotic, with t-cell immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia, anhidrotic, with t-cell immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

acromesomelic dysplasia, maroteaux type Gene Set

From OMIM Gene-Disease Associations

genes associated with the acromesomelic dysplasia, maroteaux type phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 5, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 5, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

smith-mccort dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the smith-mccort dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

craniodiaphyseal dysplasia, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniodiaphyseal dysplasia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, with myopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

septooptic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the septooptic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

acromesomelic dysplasia, hunter-thompson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the acromesomelic dysplasia, hunter-thompson type phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia, missouri type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia, missouri type phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocephaly with multiple epiphyseal dysplasia and distinctive facies Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocephaly with multiple epiphyseal dysplasia and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia tarda Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia tarda phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 1, hypohidrotic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 1, hypohidrotic, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

diastrophic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the diastrophic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia-syndactyly syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia-syndactyly syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

schneckenbecken dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the schneckenbecken dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.