| Name |
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CTD Gene-Disease Associations DatasetFrom Comparative Toxicogenomics Database Disease-gene interactions from manually curated literature |
DISEASES Curated Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Disease gene evidence scores by manual literature curation |
DISEASES Experimental Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Disease gene evidence scores by integrating experimental data (GWAS) |
DISEASES Text-mining Gene-Disease Association Evidence Scores Dataset (Archived)From DISEASES Gene-disease co-occurrence scores from text-mining biomedical abstracts |
GAD Gene-Disease Associations DatasetFrom Genetic Association Database Gene-disease associations curated from genetic association studies |
GAD High Level Gene-Disease Associations DatasetFrom Genetic Association Database Gene-disease associations curated from genetic association studies |
GWASdb SNP-Disease Associations DatasetFrom GWASdb SNP-disease association p-values curated from published GWAS |
HPO Gene-Disease Associations DatasetPhenotype-causing gene mutations of human phenotypes from disease knowledgebases |
OMIM Gene-Disease Associations DatasetFrom Online Mendelian Inheritance in Man Disease- or phenotype-causing gene mutations for heritable human diseases or phenotypes curated from biomedical publications |
PhosphoSitePlus Phosphosite-Disease Associations DatasetFrom PhosphoSitePlus Disease-phosphosite associations curated from literature |
DisGeNET Gene-Disease Associations DatasetFrom DisGeNET Gene-disease associations sourced from curated repositories, GWAS catalogues, animal models and the scientific literature |
DISEASES Curated Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Disease gene evidence scores by manual literature curation |
DISEASES Experimental Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Disease gene evidence scores by integrating experimental data (GWAS) |
DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 DatasetFrom DISEASES Gene-disease co-occurrence scores from text-mining biomedical abstracts |
RDPA Generefsum disease, adult, with increased pipecolicacidemia |
NPC2 GeneNiemann-Pick disease, type C2 This gene encodes a protein containing a lipid recognition domain. The encoded protein may function in regulating the transport of cholesterol through the late endosomal/lysosomal system. Mutations in this gene have been associated with Niemann-Pick disease, type C2 and frontal lobe atrophy. [provided by RefSeq, Jul 2008] |
NPC1 GeneNiemann-Pick disease, type C1 This gene encodes a large protein that resides in the limiting membrane of endosomes and lysosomes and mediates intracellular cholesterol trafficking via binding of cholesterol to its N-terminal domain. It is predicted to have a cytoplasmic C-terminus, 13 transmembrane domains, and 3 large loops in the lumen of the endosome - the last loop being at the N-terminus. This protein transports low-density lipoproteins to late endosomal/lysosomal compartments where they are hydrolized and released as free cholesterol. Defects in this gene cause Niemann-Pick type C disease, a rare autosomal recessive neurodegenerative disorder characterized by over accumulation of cholesterol and glycosphingolipids in late endosomal/lysosomal compartments.[provided by RefSeq, Aug 2009] |
CMT2H GeneCharcot-Marie-Tooth disease, axonal, type 2H |
CMT2G GeneCharcot-Marie-Tooth disease, axonal, type 2G |
GRD2 GeneGraves disease, susceptibility to, 2 |
GRD1 GeneGraves disease, susceptiblity to, 1 |
GRDX GeneGraves disease, susceptibility to, X-linked |
COPD14 GeneChronic obstructive pulmonary disease QTL 14 |
PDDC1 GeneParkinson disease 7 domain containing 1 Predicted to enable glyoxalase III activity. Predicted to be involved in methylglyoxal catabolic process to D-lactate via S-lactoyl-glutathione. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
CELIAC8 GeneCeliac disease, susceptibility to, 8 |
CELIAC2 Geneceliac disease 2 |
CELIAC5 GeneCeliac disease, susceptibility to, 5 |
CELIAC6 GeneCeliac disease, susceptibility to, 6 |
CELIAC7 GeneCeliac disease, susceptibility to, 7 |
AIS4 Geneautoimmune disease, susceptibility to, 4 |
COPD3 GeneChronic obstructive pulmonary disease QTL 3 |
COPD2 GeneChronic obstructive pulmonary disease QTL 2 |
COPD1 GeneChronic obstructive pulmonary disease QTL 1 |
COPD6 GeneChronic obstructive pulmonary disease QTL 6 |
COPD5 GeneChronic obstructive pulmonary disease QTL 5 |
COPD4 GeneChronic obstructive pulmonary disease QTL 4 |
COPD8 GeneChronic obstructive pulmonary disease QTL 8 |
PKHD1L1 Genepolycystic kidney and hepatic disease 1 (autosomal recessive)-like 1 Predicted to enable signaling receptor activity. Predicted to be involved in immune response. Predicted to act upstream of or within sensory perception of sound. Predicted to be located in cytosol; extracellular space; and membrane. Implicated in autosomal recessive nonsyndromic deafness. [provided by Alliance of Genome Resources, Mar 2025] |
BED GeneBornholm eye disease |
PKD1P1 Genepolycystic kidney disease 1 (autosomal dominant) pseudogene 1 |
PKD1P2 Genepolycystic kidney disease 1 (autosomal dominant) pseudogene 2 |
PKD1P3 Genepolycystic kidney disease 1 (autosomal dominant) pseudogene 3 |
PKD1P4 Genepolycystic kidney disease 1 (autosomal dominant) pseudogene 4 |
PKD1P5 Genepolycystic kidney disease 1 (autosomal dominant) pseudogene 5 |
PKD1P6 Genepolycystic kidney disease 1 (autosomal dominant) pseudogene 6 |
PKD3 Genepolycystic kidney disease 3 (autosomal dominant) |
PKD2 Genepolycystic kidney disease 2 (autosomal dominant) This gene encodes a member of the polycystin protein family. The encoded protein is a multi-pass membrane protein that functions as a calcium permeable cation channel, and is involved in calcium transport and calcium signaling in renal epithelial cells. This protein interacts with polycystin 1, and they may be partners in a common signaling cascade involved in tubular morphogenesis. Mutations in this gene are associated with autosomal dominant polycystic kidney disease type 2. [provided by RefSeq, Mar 2011] |
PKD1 Genepolycystic kidney disease 1 (autosomal dominant) This gene encodes a member of the polycystin protein family. The encoded glycoprotein contains a large N-terminal extracellular region, multiple transmembrane domains and a cytoplasmic C-tail. It is an integral membrane protein that functions as a regulator of calcium permeable cation channels and intracellular calcium homoeostasis. It is also involved in cell-cell/matrix interactions and may modulate G-protein-coupled signal-transduction pathways. It plays a role in renal tubular development, and mutations in this gene cause autosomal dominant polycystic kidney disease type 1 (ADPKD1). ADPKD1 is characterized by the growth of fluid-filled cysts that replace normal renal tissue and result in end-stage renal failure. Splice variants encoding different isoforms have been noted for this gene. Also, six pseudogenes, closely linked in a known duplicated region on chromosome 16p, have been described. [provided by RefSeq, Oct 2008] |
OED GeneOregon eye disease |
CHDS4 GeneCoronary heart disease, susceptibility to, 4 |
GBD3 Genegallbladder disease 3 |
CMTDIA GeneCharcot-Marie-Tooth disease, dominant intermediate 2 |
PDB6 GenePaget disease of bone 6 |
PDB4 GenePaget disease of bone 4 |
PDB5 GenePaget disease of bone 5 |
PDB1 GenePaget disease of bone 1 |
IBD9 Geneinflammatory bowel disease 9 |
IBD8 Geneinflammatory bowel disease 8 |
IBD3 Geneinflammatory bowel disease 3 |
IBD2 Geneinflammatory bowel disease 2 |
IBD5 Geneinflammatory bowel disease 5 |
IBD4 Geneinflammatory bowel disease 4 |
IBD7 Geneinflammatory bowel disease 7 |
IBD6 Geneinflammatory bowel disease 6 |
COPD17 GeneChronic obstructive pulmonary disease QTL 17 |
GBD2 Genegallbladder disease 2 |
PAOD1 GenePeripheral arterial occlusive disease 1 |
COPD7 GeneChronic obstructive pulmonary disease QTL 7 |
COPD9 GeneChronic obstructive pulmonary disease QTL 9 |
DDD3 GeneDowling-Degos disease 3 |
NAFLD2 GeneFatty liver disease, nonalcoholic, susceptibility to, 2 |
NAFLD1 GeneFatty liver disease 1, susceptiblity to |
EPM2A Geneepilepsy, progressive myoclonus type 2A, Lafora disease (laforin) This gene encodes a dual-specificity phosphatase and may be involved in the regulation of glycogen metabolism. The protein acts on complex carbohydrates to prevent glycogen hyperphosphorylation, thus avoiding the formation of insoluble aggregates. Loss-of-function mutations in this gene have been associated with Lafora disease, a rare, adult-onset recessive neurodegenerative disease, which results in myoclonus epilepsy and usually results in death several years after the onset of symptoms. The disease is characterized by the accumulation of insoluble particles called Lafora bodies, which are derived from glycogen. [provided by RefSeq, Jan 2018] |
PKDTS Genepolycystic kidney disease, infantile severe, with tuberous sclerosis |
AITD2 GeneAutoimmune thyroid disease, susceptibility to, 2 |
AITD1 GeneAutoimmune thyroid disease, susceptibility to, 1 |
AITD4 GeneAutoimmune thyroid disease, susceptibility to, 4 |
KWE Genekeratolytic winter erythema (Oudtshoorn skin disease) |
LOC613206 Genemyeloproliferative disease associated tumor antigen 5 |
RMD1 Generippling muscle disease 1 |
AD10 GeneAlzheimer disease-10 |
AD11 GeneAlzheimer disease-11 |
AD12 GeneAlzheimer disease 12 |
AD13 GeneAlzheimer disease-13 |
AD14 GeneAlzheimer disease 14 |
AD16 GeneAlzheimer disease 16 |
AD17 GeneAlzheimer disease 17 |
PKD1L1 Genepolycystic kidney disease 1 like 1 This gene encodes a member of the polycystin protein family containing 11 transmembrane domains, a receptor for egg jelly (REJ) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. The encoded protein may play a role in the male reproductive system. Alternative splice variants have been described but their biological nature has not been determined. [provided by RefSeq, Jul 2008] |
PKD1L2 Genepolycystic kidney disease 1-like 2 (gene/pseudogene) This gene encodes a member of the polycystin protein family. This protein may function as a G-protein-coupled component or regulator of cation channel pores. The long isoform of this protein contains 11 transmembrane domains, a latrophilin/CL-1-like GPCR proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. Alternative splicing results in multiple transcript variants encoding distinct isoforms. This gene is a polymorphic pseudogene in humans. [provided by RefSeq, May 2022] |
PKD1L3 Genepolycystic kidney disease 1-like 3 This gene encodes a member of the polycystin protein family. The encoded protein contains 11 transmembrane domains, a latrophilin/CL-1-like GPCR proteolytic site (GPS) domain, and a polycystin-1, lipoxygenase, alpha-toxin (PLAT) domain. This protein may function as a component of cation channel pores.[provided by RefSeq, Apr 2009] |
HDPA GeneHodgkin disease, susceptibility, pseudoautosomal |
AD6 GeneAlzheimer disease 6 |
AD7 GeneAlzheimer disease 7 |
AD5 GeneAlzheimer disease 5 |
AD8 GeneAlzheimer disease 8 |
AD9 GeneAlzheimer disease 9 |
PARK16 GeneParkinson disease 16 (susceptibility) |
PARK10 GeneParkinson disease 10 (susceptibility) |
PARK12 GeneParkinson disease 12 (susceptibility) |
HSCR9 GeneHirschsprung disease, susceptibility to, 9 |
HSCR8 GeneHirschsprung disease modifier 2 |
HSCR5 GeneHirschsprung disease, susceptibility to, 5 The disorder described by Hirschsprung (1888) and known as Hirschsprung disease or aganglionic megacolon is characterized by congenital absence of intrinsic ganglion cells in the myenteric (Auerbach) and submucosal (Meissner) plexuses of the gastrointestinal tract. Patients are diagnosed with the short-segment form (S-HSCR, approximately 80% of cases) when the aganglionic segment does not extend beyond the upper sigmoid, and with the long-segment form (L-HSCR) when aganglionosis extends proximal to the sigmoid. Total colonic aganglionosis and total intestinal HSCR also occur (Amiel et al., 2008 [PubMed 17965226]). Isolated HSCR appears to be of complex nonmendelian inheritance with low sex-dependent penetrance and variable expression according to the length of the aganglionic segment, suggestive of the involvement of one or more genes with low penetrance (Amiel et al., 2008 [PubMed 17965226]). For a general description and a discussion of genetic heterogeneity of Hirschsprung disease (HSCR), see MIM 142623.[supplied by OMIM, Feb 2011] |
HSCR7 GeneHirschsprung disease, short-segment, 3 |
HSCR6 GeneHirschsprung disease, short-segment, 2 |
IBD27 GeneInflammatory bowel disease-27 |
IBD20 GeneInflammatory bowel disease-20 |
IBD21 GeneInflammatory bowel disease-21 |
IBD22 GeneInflammatory bowel disease-22 |
IBD23 GeneInflammatory bowel disease-23 |
IBD24 GeneInflammatory bowel disease-24 |
IBD25 GeneInflammatory bowel disease-25 |
IBD26 GeneInflammatory bowel disease-26 |
CCAL1 Genechondrocalcinosis 1 (calcium pyrophosphate-deposition disease, early onset osteoarthritis) |
PARK3 GeneParkinson disease 3 (autosomal dominant, Lewy body) |
CELIAC9 GeneCeliac disease, susceptibility to, 9 |
CTD GeneCoats disease |
AD15 GeneAlzheimer disease-15 |
COPD13 GeneChronic obstructive pulmonary disease QTL 13 |
COPD12 GeneChronic obstructive pulmonary disease QTL 12 |
COPD11 GeneChronic obstructive pulmonary disease QTL 11 |
COPD10 GeneChronic obstructive pulmonary disease QTL 10 |
COPD16 GeneChronic obstructive pulmonary disease QTL 16 |
COPD15 GeneChronic obstructive pulmonary disease QTL 15 |
COPD19 GeneChronic obstructive pulmonary disease QTL 19 |
COPD18 GeneChronic obstructive pulmonary disease QTL 18 |
MYMY1 Genemoyamoya disease 1 |
MYMY3 Genemoyamoya disease 3 |
MYMY4 GeneMoyamoya disease 4 |
COPD GenePulmonary disease, chronic obstructive, severe early-onset |
CHDS3 GeneCoronary heart disease, susceptibility to, 3 |
CHDS2 GeneCoronary heart disease, susceptibility to, 2 |
CHDS1 GeneCoronary heart disease, susceptibility to, 1 |
CHDS9 GeneCoronary heart disease, suscpetibility to, 9 |
CHDS8 GeneCoronary heart disease, susceptibility to, 8 |
IBD11 GeneInflammatory bowel disease 11 |
IBD12 GeneInflammatory bowel disease 12 |
IBD15 GeneInflammatory bowel disease-15 |
IBD16 GeneInflammatory bowel disease-16 |
IBD19 GeneInflammatory bowel disease 19 |
IBD18 GeneInflammatory bowel disease-18 |
NDP GeneNorrie disease (pseudoglioma) This gene encodes a secreted protein with a cystein-knot motif that activates the Wnt/beta-catenin pathway. The protein forms disulfide-linked oligomers in the extracellular matrix. Mutations in this gene result in Norrie disease and X-linked exudative vitreoretinopathy. [provided by RefSeq, Feb 2009] |
PKHD1 Genepolycystic kidney and hepatic disease 1 (autosomal recessive) The protein encoded by this gene is predicted to have a single transmembrane (TM)-spanning domain and multiple copies of an immunoglobulin-like plexin-transcription-factor domain. Alternative splicing results in two transcript variants encoding different isoforms. Other alternatively spliced transcripts have been described, but the full length sequences have not been determined. Several of these transcripts are predicted to encode truncated products which lack the TM and may be secreted. Mutations in this gene cause autosomal recessive polycystic kidney disease, also known as polycystic kidney and hepatic disease-1. [provided by RefSeq, Jul 2008] |
PKD2L2 Genepolycystic kidney disease 2-like 2 Predicted to enable calcium channel activity. Predicted to be involved in detection of mechanical stimulus. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PKD2L1 Genepolycystic kidney disease 2-like 1 This gene encodes a member of the polycystin protein family. The encoded protein contains multiple transmembrane domains, and cytoplasmic N- and C-termini. The protein may be an integral membrane protein involved in cell-cell/matrix interactions. This protein functions as a calcium-regulated nonselective cation channel. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011] |
COPD28 GeneChronic obstructive pulmonary disease QTL 28 |
COPD29 GeneChronic obstructive pulmonary disease QTL 29 |
COPD22 GeneChronic obstructive pulmonary disease QTL 22 |
COPD23 GeneChronic obstructive pulmonary disease QTL 23 |
COPD20 GeneChronic obstructive pulmonary disease QTL 20 |
COPD21 GeneChronic obstructive pulmonary disease QTL 21 |
COPD26 GeneChronic obstructive pulmonary disease QTL 26 |
COPD27 GeneChronic obstructive pulmonary disease QTL 27 |
COPD24 GeneChronic obstructive pulmonary disease QTL 24 |
COPD25 GeneChronic obstructive pulmonary disease QTL 25 |
CELIAC12 GeneCeliac disease, susceptibility to, 12 |
CELIAC13 GeneCeliac disease, susceptibility to, 13 |
CELIAC10 GeneCeliac disease, susceptibility to, 10 |
CELIAC11 GeneCeliac disease, susceptibility to, 11 |
Fibrocystic Disease Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrocystic Disease Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
breast fibrocystic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease breast fibrocystic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
breast neoplasms; fibrocystic breast disease; mammary neoplasms; neoplasm invasiveness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; fibrocystic breast disease; mammary neoplasms; neoplasm invasiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fibrocystic lung disease Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the fibrocystic lung disease phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
Fibrocystic Breast Disease Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Fibrocystic Breast Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Breast Fibrocystic Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Breast Fibrocystic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonproliferative Fibrocystic Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonproliferative Fibrocystic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Breast fibrocystic disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast fibrocystic disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-proliferative fibrocystic change of the breast Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease non-proliferative fibrocystic change of the breast in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
fibrocystic Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term fibrocystic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Breast Fibrocystic Change, Proliferative Type Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Breast Fibrocystic Change, Proliferative Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrocystic Dysplasia Of Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrocystic Dysplasia Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
non-proliferative fibrocystic change of the breast Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-proliferative fibrocystic change of the breast in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Proliferative type fibrocystic change of breast Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Proliferative type fibrocystic change of breast in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
pancreas disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease pancreas disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
pancreas disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pancreas disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
endocrine pancreas disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endocrine pancreas disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pancreas disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pancreas disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pancreas disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease pancreas disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
Pancreas disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Pancreas disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pancreas disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pancreas disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Endocrine pancreas disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Endocrine pancreas disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
coronary artery disease; coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves' disease; hashimoto disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; graves disease; hashimoto disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; disease susceptibility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves' disease; hashimoto disease; hypothyroidism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colitis; crohn disease; crohn's disease; disease models, animal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; graft vs host disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; graft vs host disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pancreas Gene SetFrom BioGPS Human Cell Type and Tissue Gene Expression Profiles genes with high or low expression in Pancreas relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset. |
pancreas Gene SetFrom BioGPS Mouse Cell Type and Tissue Gene Expression Profiles genes with high or low expression in pancreas relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset. |
pancreas adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pancreas adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adenosquamous pancreas carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adenosquamous pancreas carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pancreas lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pancreas lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
colloid carcinoma of the pancreas Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colloid carcinoma of the pancreas in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
tumor of exocrine pancreas Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tumor of exocrine pancreas in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pancreas divisum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pancreas divisum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pancreas adenocarcinomas Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pancreas adenocarcinomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pancreas Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term pancreas in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Type 2 diabetes mellitus_Endocrine Pancreas - Islet Cell of Langerhans - Beta Cell (MMHCC)_GSE6428 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Type 2 diabetes mellitus_Endocrine Pancreas - Islet Cell of Langerhans - Beta Cell (MMHCC)_GSE6428 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
GLIS3_KO_GDS3812_500_mouse_Embryonic pancreas at E15.5 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the GLIS3_KO_GDS3812_500_mouse_Embryonic pancreas at E15.5 gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
Rkip1_KO_GDS4331_15_mouse_C57BL/C pancreas Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Rkip1_KO_GDS4331_15_mouse_C57BL/C pancreas gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
endocrine pancreas development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the endocrine pancreas development biological process from the curated GO Biological Process Annotations 2015 dataset. |
pancreas development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pancreas development biological process from the curated GO Biological Process Annotations 2015 dataset. |
pancreas morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pancreas morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
branching involved in pancreas morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the branching involved in pancreas morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
exocrine pancreas development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the exocrine pancreas development biological process from the curated GO Biological Process Annotations 2015 dataset. |
pancreas Gene SetFrom GTEx Tissue Gene Expression Profiles genes with high or low expression in pancreas relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. |
neoplasm of the pancreas Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neoplasm of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pancreas Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
pancreas Gene SetFrom HPA Tissue Gene Expression Profiles genes with high or low expression in pancreas relative to other tissues from the HPA Tissue Gene Expression Profiles dataset. |
pancreas Gene SetFrom HPA Tissue Protein Expression Profiles proteins with high or low expression in pancreas relative to other tissues from the HPA Tissue Protein Expression Profiles dataset. |
abnormality of pancreas morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pancreas size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pancreas size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hyperechogenic pancreas Gene SetFrom HPO Gene-Disease Associations genes associated with the hyperechogenic pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of exocrine pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of exocrine pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the pancreas Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of endocrine pancreas physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of endocrine pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
annular pancreas Gene SetFrom HPO Gene-Disease Associations genes associated with the annular pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the pancreas Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pancreas Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Soluble liver antigen/liver pancreas antigen Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Soluble liver antigen/liver pancreas antigen protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
decreased pancreas weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased pancreas weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas regeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas fibrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pancreas adenoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pancreas adenoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged pancreas Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged pancreas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas cysts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas cysts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas mesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
acute pancreas inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the acute pancreas inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased pancreas regeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased pancreas regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas necrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ectopic pancreas Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ectopic pancreas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endocrine pancreas development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endocrine pancreas development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal exocrine pancreas morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal exocrine pancreas morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pancreas Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pancreas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pancreas iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pancreas iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pancreas apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pancreas apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
exocrine pancreas atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pancreas weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pancreas weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pancreas tumor incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pancreas tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent pancreas Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent pancreas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
chronic pancreas inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the chronic pancreas inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endocrine pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endocrine pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
exocrine pancreas hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
annular pancreas Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the annular pancreas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas inflammation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal exocrine pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal exocrine pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas iron level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
exocrine pancreas hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas lipomatosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas lipomatosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endocrine pancreas morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endocrine pancreas morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas Gene SetFrom ProteomicsDB Cell Type and Tissue Protein Expression Profiles proteins with high or low expression in pancreas relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset. |
Pancreas Gene SetFrom Roadmap Epigenomics Cell and Tissue Gene Expression Profiles genes with high or low expression in Pancreas relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue Gene Expression Profiles dataset. |
pancreas Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue pancreas from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
endocrine pancreas Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue endocrine pancreas from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
pancreas Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue pancreas in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
endocrine pancreas Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue endocrine pancreas in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
pancreas Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue pancreas in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
endocrine pancreas Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue endocrine pancreas in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
exocrine pancreas Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue exocrine pancreas in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Pancreas-b cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-b cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-endothelial cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-fibroblast Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-fibroblast relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-mast cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-mast cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-myeloid cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-myeloid cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-nk cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-nk cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-pancreatic acinar cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-pancreatic acinar cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-pancreatic alpha cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-pancreatic alpha cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-pancreatic beta cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-pancreatic beta cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-pancreatic delta cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-pancreatic delta cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-pancreatic ductal cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-pancreatic ductal cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-pancreatic pp cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-pancreatic pp cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-pancreatic stellate cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-pancreatic stellate cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-plasma cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-plasma cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pancreas-t cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Pancreas-t cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Congenital Hypoplasia Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypoplasia Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Exocrine Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Exocrine Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pearson'S Marrow-Pancreas Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pearson'S Marrow-Pancreas Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fibrosis Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fibrosis Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Tumor Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Tumor Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Solid Pseudopapillary Tumour Of The Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Solid Pseudopapillary Tumour Of The Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Necrosis Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Necrosis Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Neoplasm Of Head Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Neoplasm Of Head Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Malignant Neoplasm Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Malignant Neoplasm Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neuroendocrine Tumor Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neuroendocrine Tumor Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Absence Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pancreas Divisum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pancreas Divisum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bilateral Pheochromocytoma And Islet Cell Adenoma Of The Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Pheochromocytoma And Islet Cell Adenoma Of The Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Annular Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Annular Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colloid Carcinoma Of The Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colloid Carcinoma Of The Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ectopic Pancreas Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ectopic Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pancreas Exocrine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pancreas Exocrine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperechogenic Pancreas Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperechogenic Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Exocrine Pancreas Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Exocrine Pancreas Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Endocrine Pancreas Physiology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Endocrine Pancreas Physiology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Pancreas Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
exocrine pancreas development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the exocrine pancreas development biological process from the curated GO Biological Process Annotations 2023 dataset. |
pancreas development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the pancreas development biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal pancreas morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal exocrine pancreas morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal exocrine pancreas morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent pancreas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas cyst Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas cyst phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pancreas tumor incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pancreas tumor incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pancreas apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pancreas apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endocrine pancreas development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endocrine pancreas development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas fibrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas fibrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small pancreas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged pancreas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
acute pancreas inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the acute pancreas inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased pancreas weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pancreas weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
exocrine pancreas hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the exocrine pancreas hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endocrine pancreas morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endocrine pancreas morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ectopic pancreas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas necrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
exocrine pancreas hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the exocrine pancreas hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas secretion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed pancreas regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed pancreas regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas lipomatosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas lipomatosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
exocrine pancreas atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
annular pancreas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the annular pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pancreas iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pancreas iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired pancreas regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired pancreas regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pancreas adenoma incidence Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pancreas adenoma incidence phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas mesenchyme morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas mesenchyme morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pancreas weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pancreas weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
chronic pancreas inflammation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the chronic pancreas inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal endocrine pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endocrine pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased pancreas iron level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pancreas iron level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal exocrine pancreas physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal exocrine pancreas physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal dorsal pancreas topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dorsal pancreas topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ventral pancreas morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ventral pancreas morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreas regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ventral pancreas topology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ventral pancreas topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent ventral pancreas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent ventral pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small ventral pancreas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small ventral pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small dorsal pancreas Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small dorsal pancreas phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pancreas atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreas morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal pancreas morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
enlarged pancreas Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the enlarged pancreas phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
small pancreas Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the small pancreas phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
absent pancreas Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the absent pancreas phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Pancreas Gene SetFrom GTEx Tissue Gene Expression Profiles 2023 genes with high or low expression in Pancreas relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset. |
GTEx Pancreas 20-29 vs 60-69 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Pancreas 20-29 vs 60-69 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
GTEx Pancreas 20-29 vs 50-59 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Pancreas 20-29 vs 50-59 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
GTEx Pancreas 20-29 vs 40-49 Gene SetFrom GTEx Tissue-Specific Aging Signatures genes with high or low expression in GTEx Pancreas 20-29 vs 40-49 relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset. |
Human - Pancreas - L1 - cycling Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - cycling cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - immune Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - immune cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - quiescent stellate Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - quiescent stellate cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - endothelial Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - endothelial cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - schwann Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - schwann cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - activated stellate Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - activated stellate cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - epsilon islet cell Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - epsilon islet cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - gamma islet cell Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - gamma islet cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - delta islet cell Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - delta islet cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - ductal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - ductal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - acinar Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - acinar cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - beta islet cell Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - beta islet cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Pancreas - L1 - alpha islet cell Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Pancreas - L1 - alpha islet cell cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Stromal cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Lymphatic endothelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Myeloid cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Vascular endothelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Erythroblasts Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-ENS glia Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Lymphoid cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Mesothelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Smooth muscle cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Islet endocrine cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Islet endocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Acinar cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Acinar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-Ductal cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Ductal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-ENS neurons Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Pancreas-CCL19_CCL21 positive cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-CCL19_CCL21 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
exocrine pancreas development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the exocrine pancreas development biological process from the curated GO Biological Process Annotations 2025 dataset. |
pancreas development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the pancreas development biological process from the curated GO Biological Process Annotations 2025 dataset. |
Malignant exocrine pancreas neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Malignant exocrine pancreas neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant exocrine pancreas neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant exocrine pancreas neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Annular pancreas Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Annular pancreas in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Colloid carcinoma of the pancreas Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colloid carcinoma of the pancreas in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pancreas lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pancreas lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mucinous cystadenocarcinoma of pancreas Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mucinous cystadenocarcinoma of pancreas in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pancreas sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pancreas sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pancreas Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Pancreas from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Endocrine pancreas Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Endocrine pancreas from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Endocrine pancreas Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Endocrine pancreas in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Pancreas Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Pancreas in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Pancreas Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Pancreas in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Endocrine pancreas Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Endocrine pancreas in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Exocrine pancreas Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Exocrine pancreas in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Malignant tumor of pancreas Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Malignant tumor of pancreas phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Carcinoma of pancreas Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Carcinoma of pancreas phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neuroendocrine tumor of pancreas Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuroendocrine tumor of pancreas phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pancreas volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pancreas volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pancreas fat Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pancreas fat phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
crohn disease; crohn's disease; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; melanoma; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart disease, ischemic; peripheral arterial disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; pulmonary embolism; pulmonary embolisms; syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; hashimoto disease; hyperthyroidism; hypothyroidism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease; hyperthyroidism; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; atherosclerosis; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; granuloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; granuloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; familial mediterranean fever Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; familial mediterranean fever in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypercholesterolemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; myocardial infarction; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liver disease; wilson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease liver disease; wilson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic obstructive pulmonary disease/copd; bronchiectatic disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic obstructive pulmonary disease/copd; bronchiectatic disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; dna damage; genomic instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; dna damage; genomic instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hemochromatosis; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hemochromatosis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinson's disease ; alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinson's disease ; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart disease, ischemic; cerebrovascular disease, ischemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; duodenal diseases; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; sarcoidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; sarcoidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison's disease; graves' disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison's disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney disease; vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves ophthalmopathy; hashimoto disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; addison's disease; graves' disease; thyroiditis, chronic lymphocytic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; olfaction disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; hashimoto disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileal diseases; intestinal fistula; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; autoimmune diseases; graves disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; autoimmune diseases; graves disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; crohn's disease; asthma; malaria; malaria infection; kawasaki disease; psoriasis vulgaris; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; mercury poisoning, nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; mercury poisoning, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis; colitis, ulcerative; crohn disease; crohn's disease; ileitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; dementia, vascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; dementia; neurodegenerative diseases; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; neurodegenerative diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; influenza; influenza, human; postoperative complications; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; colitis, ulcerative; crohn disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; crohn disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adult-onset still disease; still's disease, adult-onset Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; obesity; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graft vs host disease; hematologic neoplasms; inflammatory bowel disease, nos; inflammatory bowel diseases; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves' disease; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amnesia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amnesia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; coronary disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; coronary disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular disease; cerebrovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; cholelithiasis; colitis; crohn disease; crohn's disease; erythema nodosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; brain ischemia; cardiovascular diseases; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gaucher disease; nervous system diseases; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gaucher disease; nervous system diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease calcinosis; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; metabolic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; metabolic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves' disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; coronary restenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; myocardial infarction; postoperative complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; osteomyelitis; unspecified osteomyelitis nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graft-versus-host disease; psoriasis; celiac disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graft-versus-host disease; psoriasis; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease parkinson's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease parkinson's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colonic neoplasms; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina pectoris, variant; chest pain; coronary disease; coronary heart disease; myocardial infarction; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cardiovascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart disease, ischemic; peripheral vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart disease, ischemic; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
angina pectoris; coronary disease; coronary heart disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina pectoris; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; spondylitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; spondylitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; gastrointestinal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; gastrointestinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gaucher disease; legg-perthes disease; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gaucher disease; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn's disease; ulcerative colitis; inflammatory bowel disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn's disease; ulcerative colitis; inflammatory bowel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; postoperative complications; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; inflammation; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular disease; periodontal disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; crohn disease; crohn's disease; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; coronary disease; coronary heart disease; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary disease; coronary heart disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; heart failure; hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; dyslipidemias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; dyslipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; osteoporosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; disease susceptibility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; disease susceptibility; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; disease susceptibility; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypertriglyceridemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; addison's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; mucocutaneous lymph node syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hypercholesterolemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroiditis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; hemochromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; stroke; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; rheumatoid spondylitis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; ileal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; ileal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
parkinsons disease; alzheimers disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease parkinsons disease; alzheimers disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; cardiovascular diseases; coronary disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease communicable diseases; coronary disease; coronary heart disease; degenerative arthropathy ; diabetes mellitus; hyperparathyroidism; neoplasms; osteoarthritis; osteoporosis, postmenopausal; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; coronary artery disease; hyperlipidemias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; coronary artery disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; inflammation; myocardial infarction; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; coronary disease; coronary heart disease; hypertension; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; hyperplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadaver; coronary disease; coronary heart disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadaver; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rheumatoid arthritis; crohn's disease; diabetes, type 1; celiac disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
common variable immunodeficiency; crohn disease; crohn's disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease common variable immunodeficiency; crohn disease; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; arteriosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; arteriosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; intestinal obstruction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; parkinson's disease; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
constriction, pathologic; crohn disease; crohn's disease; fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetic angiopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; dilatation, pathologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; dilatation, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia, vascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lewy body disease; parkinson disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lewy body disease; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyloidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperlipidemias Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sanhoff disease; tay-sachs disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sanhoff disease; tay-sachs disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hypertension, portal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperhomocysteinemia; myocardial ischemia; recurrence; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; postoperative complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fatigue; inflammation; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; postoperative complications; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; postoperative complications; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hemochromatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; delirium; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; delirium; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease/coronary artery disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease/coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; coronary disease; coronary heart disease; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; hallucinations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; growth disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; graves ophthalmopathy; graves' disease; thyroid associated opthalmopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; lewy body disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; heart disease, ischemic; cerebrovascular disease, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; lewy body disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hyperlipidemias; hyperlipoproteinemia type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary heart disease; myocardial infarction; stroke; cerebrovascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary heart disease; myocardial infarction; stroke; cerebrovascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves disease; hashimoto disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves disease; hashimoto disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hepatitis c; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
addison disease; addison's disease; autoimmune diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease addison disease; addison's disease; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetes mellitus; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetes mellitus; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease creutzfeldt-jakob disease; gerstmann-straussler-scheinker disease; insomnia, fatal familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ahg deficiency disease; hemophilia a; hiv infections; sexually transmitted diseases, viral; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
celiac disease; colitis, ulcerative; crohn disease; psoriasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease celiac disease; colitis, ulcerative; crohn disease; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer's disease; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; sclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune thyroid disease; thyroid disease, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune thyroid disease; thyroid disease, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; genetic predisposition to disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; atherosclerosis; coronary disease; coronary heart disease; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; neural tube defects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; neural tube defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; diabetic cardiomyopathies; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic angiopathies; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; cutaneous fistula; rectal fistula Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; cutaneous fistula; rectal fistula in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; autoimmune diseases; coronary disease; coronary heart disease; hypertension; lupus erythematosus, systemic; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; graves disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; spondylarthropathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; spondylarthropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Crohn's disease and celiac disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Cardiovascular Disease+Pulmonary Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cardiovascular Disease+Pulmonary Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Parkinson's disease or first degree relation to individual with Parkinson's disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Parkinson's disease or first degree relation to individual with Parkinson's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alzheimer's disease or family history of Alzheimer's disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alzheimer's disease or family history of Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Crohn's disease and celiac disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Crohn's disease and celiac disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors Gene SetFrom Biocarta Pathways proteins participating in the inhibition of huntingtons disease neurodegeneration by histone deacetylase inhibitors pathway from the Biocarta Pathways dataset. |
deregulation of cdk5 in alzheimers disease Gene SetFrom Biocarta Pathways proteins participating in the deregulation of cdk5 in alzheimers disease pathway from the Biocarta Pathways dataset. |
alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene SetFrom Biocarta Pathways proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset. |
Parkinson disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Premature coronary artery disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Premature coronary artery disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Jakob-Creutzfeldt disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Jakob-Creutzfeldt disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, X-linked dominant, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked dominant, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Maple syrup urine disease type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher's disease, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher's disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stargardt Disease 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stargardt Disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4H Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4J Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4J phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4G Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4G phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Norum disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Norum disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Salla disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Salla disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Worth disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Worth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ménière's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ménière's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Maple syrup urine disease, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Acute neuronopathic Gaucher's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Acute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IVF Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IVF phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, dominant intermediate F Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate F phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, dominant intermediate E Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate E phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, dominant intermediate C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type IXa1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type IXa1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autosomal recessive hypophosphatemic bone disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory bowel disease 25, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory bowel disease 25, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Moyamoya disease 6 with achalasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Moyamoya disease 6 with achalasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IV, congenital neuromuscular Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4B3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 4B1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 4B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brain small vessel disease with hemorrhage Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
RRM2B-related mitochondrial disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the RRM2B-related mitochondrial disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Phytanic acid storage disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Phytanic acid storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 20, early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphosphatasemia with bone disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasemia with bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 2A2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chylomicron retention disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chylomicron retention disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Basal ganglia disease, biotin-responsive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Basal ganglia disease, biotin-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coronary artery disease, autosomal dominant 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coronary artery disease, autosomal dominant 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 18 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hepatic venoocclusive disease with immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hepatic venoocclusive disease with immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Triglyceride storage disease with ichthyosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Triglyceride storage disease with ichthyosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cowden disease 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cowden disease 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type II, infantile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type II, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 2A1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IF Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IE Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type ID Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IC Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IB Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IB phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type IA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alzheimer's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alzheimer's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Schindler disease, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Schindler disease, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Schindler disease, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Schindler disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-pick disease, intermediate, protracted neurovisceral Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-pick disease, intermediate, protracted neurovisceral phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 6, autosomal recessive early-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pseudo von Willebrand disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, juvenile type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, juvenile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Darier disease, segmental Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Darier disease, segmental phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Naxos disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Naxos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, axonal, type 2s Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2s phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, axonal, type 2r Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2r phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, axonal, type 2q Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, axonal, type 2q phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leiner disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leiner disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polycystic kidney disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dowling-degos disease 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dowling-degos disease 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease, atypical, due to saposin C deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor II deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease 0, muscle Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease 0, muscle phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Subacute neuronopathic Gaucher's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Subacute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, X-linked recessive, type 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, X-linked recessive, type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, X-linked recessive, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Testicular anomalies with or without congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lafora disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lafora disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease, type B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease, type A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease, type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type X Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type X phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tangier disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tangier disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inflammatory skin and bowel disease, neonatal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cole disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cole disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 8, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 8, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IXa2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXa2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Refsum disease, adult, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Refsum disease, adult, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital heart disease, multiple types, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Werdnig-Hoffmann disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Werdnig-Hoffmann disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, recessive intermediate B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 15 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, dominant intermediate b, with neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease 19, juvenile-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease 19, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NIEMANN-PICK DISEASE, TYPE C1, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease type C2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Niemann-Pick disease type C1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Niemann-Pick disease type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cholestanol storage disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cholestanol storage disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cowden disease 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cowden disease 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tay-sachs disease, juvenile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tay-sachs disease, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IIIa Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIa phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Stargardt disease 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stargardt disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor IX deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, adult type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease, perinatal lethal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, perinatal lethal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alexander's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alexander's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lethal arthrogryposis with anterior horn cell disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type 1A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dowling-Degos disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dowling-Degos disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tay-Sachs disease, B1 variant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease, B1 variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mast cell disease, systemic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mast cell disease, systemic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polycystic kidney disease, adult type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease dominant intermediate 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease dominant intermediate 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neutral lipid storage disease with myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NIEMANN-PICK DISEASE, TYPE C1, JUVENILE FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, infantile Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, infantile phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor XI deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Maple syrup urine disease type 1A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Maple syrup urine disease type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease, type VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease XV Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease XV phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemoglobin H disease, nondeletional Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemoglobin H disease, nondeletional phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IXb Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXb phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IXc Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXc phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease, type VI Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle eye brain disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscle eye brain disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Addison's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Addison's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital cystic disease of liver Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pancreatic agenesis and congenital heart disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lhermitte-Duclos disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lhermitte-Duclos disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kugelberg-Welander disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kugelberg-Welander disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Darier disease, acral hemorrhagic type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Darier disease, acral hemorrhagic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Wilson's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Wilson's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, recessive intermediate d Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate d phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, recessive intermediate c Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate c phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, recessive intermediate A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, recessive intermediate A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease, type II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IIIc Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIc phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IIIb Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IIIb phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease ganglioneuroblastoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease ganglioneuroblastoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Oguchi's disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Oguchi's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Kanzaki disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Kanzaki disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aortic valve disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intermediate maple syrup urine disease type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intermediate maple syrup urine disease type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fish-eye disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fish-eye disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, chronic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, chronic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polycystic kidney disease, infantile type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Central core disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Central core disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor VIII deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tay-Sachs disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 2N Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2N phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease, type 2M Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease, type 2M phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tay-Sachs disease, variant AB Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tay-Sachs disease, variant AB phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sialic acid storage disease, severe infantile type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sialic acid storage disease, severe infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2K Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2K phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
I cell disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the I cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoimmune disease, multisystem, infantile-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
GLYCOGEN STORAGE DISEASE II, ADULT FORM Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the GLYCOGEN STORAGE DISEASE II, ADULT FORM phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease type III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Medullary cystic kidney disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Medullary cystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Danon disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Danon disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dent disease 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dent disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dent disease 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dent disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease IXd Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease IXd phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glycogen storage disease, type V Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glycogen storage disease, type V phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Autoimmune disease, syndromic multisystem Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Autoimmune disease, syndromic multisystem phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2J Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2F Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Charcot-Marie-Tooth disease type 2P Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Charcot-Marie-Tooth disease type 2P phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dent Disease 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dent Disease 2 from the curated CTD Gene-Disease Associations dataset. |
Pick Disease of the Brain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pick Disease of the Brain from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 10 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 12 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 13 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 14 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 15 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 15 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 18 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 18 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 19 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 19 from the curated CTD Gene-Disease Associations dataset. |
Huntington Disease-Like 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset. |
Parkinson disease 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson disease 9 from the curated CTD Gene-Disease Associations dataset. |
Oguchi disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Oguchi disease from the curated CTD Gene-Disease Associations dataset. |
Gaucher Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease from the curated CTD Gene-Disease Associations dataset. |
Tay-Sachs Disease, AB Variant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tay-Sachs Disease, AB Variant from the curated CTD Gene-Disease Associations dataset. |
Naxos disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Naxos disease from the curated CTD Gene-Disease Associations dataset. |
Huntington Disease-Like 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease-Like 1 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2K Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2K from the curated CTD Gene-Disease Associations dataset. |
Carbamoyl-Phosphate Synthase I Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carbamoyl-Phosphate Synthase I Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
Chylomicron retention disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chylomicron retention disease from the curated CTD Gene-Disease Associations dataset. |
Cholesterol Ester Storage Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cholesterol Ester Storage Disease from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 6 from the curated CTD Gene-Disease Associations dataset. |
Addison Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Addison Disease from the curated CTD Gene-Disease Associations dataset. |
Alexander Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alexander Disease from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 16 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 16 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 17 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 17 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 7 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 4 from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease 0, Liver Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease 0, Liver from the curated CTD Gene-Disease Associations dataset. |
Tangier Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tangier Disease from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 1C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1C from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 26 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 26 from the curated CTD Gene-Disease Associations dataset. |
Pigmented Nodular Adrenocortical Disease, Primary, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 1 from the curated CTD Gene-Disease Associations dataset. |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Dominant Intermediate D Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate D from the curated CTD Gene-Disease Associations dataset. |
Hartnup Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hartnup Disease from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 1D Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1D from the curated CTD Gene-Disease Associations dataset. |
Intervertebral disc disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intervertebral disc disease from the curated CTD Gene-Disease Associations dataset. |
Von Willebrand disease, platelet type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Von Willebrand disease, platelet type from the curated CTD Gene-Disease Associations dataset. |
Coronary Artery Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Artery Disease from the curated CTD Gene-Disease Associations dataset. |
Machado-Joseph Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Machado-Joseph Disease from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease from the curated CTD Gene-Disease Associations dataset. |
Papillon-Lefevre Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Papillon-Lefevre Disease from the curated CTD Gene-Disease Associations dataset. |
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset. |
Moyamoya Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Moyamoya Disease from the curated CTD Gene-Disease Associations dataset. |
Gilbert Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gilbert Disease from the curated CTD Gene-Disease Associations dataset. |
Congenital thrombotic disease, due to Protein C deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Disease, Chronic Obstructive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Disease, Chronic Obstructive from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 14 from the curated CTD Gene-Disease Associations dataset. |
Coronary Artery Disease, Autosomal Dominant 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 9 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 11 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 16 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 16 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 12 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 10 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, X-linked, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked, 1 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2a1 from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease 0, Muscle Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease 0, Muscle from the curated CTD Gene-Disease Associations dataset. |
Basal ganglia disease, biotin-responsive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Basal ganglia disease, biotin-responsive from the curated CTD Gene-Disease Associations dataset. |
Non-alcoholic Fatty Liver Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Non-alcoholic Fatty Liver Disease from the curated CTD Gene-Disease Associations dataset. |
Graves Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Graves Disease from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Axonal, Type 2A2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2A2 from the curated CTD Gene-Disease Associations dataset. |
Hepatic Veno-Occlusive Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset. |
Hepatic venoocclusive disease with immunodeficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatic venoocclusive disease with immunodeficiency from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 25, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 25, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative from the curated CTD Gene-Disease Associations dataset. |
Stargardt disease 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Stargardt disease 3 from the curated CTD Gene-Disease Associations dataset. |
Stargardt disease 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Stargardt disease 4 from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Type IV Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type IV from the curated CTD Gene-Disease Associations dataset. |
Refsum Disease, Infantile Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Refsum Disease, Infantile from the curated CTD Gene-Disease Associations dataset. |
Polycystic liver disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycystic liver disease from the curated CTD Gene-Disease Associations dataset. |
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 8, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset. |
Celiac Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Celiac Disease from the curated CTD Gene-Disease Associations dataset. |
Genetic Predisposition to Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genetic Predisposition to Disease from the curated CTD Gene-Disease Associations dataset. |
Dimauro disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dimauro disease from the curated CTD Gene-Disease Associations dataset. |
PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease IXB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IXB from the curated CTD Gene-Disease Associations dataset. |
Coronary Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Disease from the curated CTD Gene-Disease Associations dataset. |
AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease, Secondary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease, Secondary from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Demyelinating, Type 1e from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Type 4j Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4j from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Dominant Intermediate A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate A from the curated CTD Gene-Disease Associations dataset. |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset. |
Hirschsprung Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset. |
GALLBLADDER DISEASE 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease GALLBLADDER DISEASE 1 from the curated CTD Gene-Disease Associations dataset. |
Acute Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Acute Disease from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 3, Autosomal Dominant Lewy Body Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 3, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset. |
Brain Small Vessel Disease with Hemorrhage Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset. |
Ornithine Carbamoyltransferase Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ornithine Carbamoyltransferase Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease, Type IXD Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease, Type IXD from the curated CTD Gene-Disease Associations dataset. |
PARKINSON DISEASE 5, AUTOSOMAL DOMINANT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 5, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset. |
GLYCOGEN STORAGE DISEASE IXa1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE IXa1 from the curated CTD Gene-Disease Associations dataset. |
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease XII Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease XII from the curated CTD Gene-Disease Associations dataset. |
Legionnaires' Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Legionnaires' Disease from the curated CTD Gene-Disease Associations dataset. |
Hepatorenal form of glycogen storage disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatorenal form of glycogen storage disease from the curated CTD Gene-Disease Associations dataset. |
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset. |
Schindler Disease, Type I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Schindler Disease, Type I from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Veno-Occlusive Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Veno-Occlusive Disease from the curated CTD Gene-Disease Associations dataset. |
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 4A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4A from the curated CTD Gene-Disease Associations dataset. |
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset. |
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 4 from the curated CTD Gene-Disease Associations dataset. |
Huntington Disease-Like 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease-Like 3 from the curated CTD Gene-Disease Associations dataset. |
Refsum Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Refsum Disease from the curated CTD Gene-Disease Associations dataset. |
Aland Island Eye Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aland Island Eye Disease from the curated CTD Gene-Disease Associations dataset. |
Bowen's Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bowen's Disease from the curated CTD Gene-Disease Associations dataset. |
Hodgkin Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hodgkin Disease from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II from the curated CTD Gene-Disease Associations dataset. |
Niemann-Pick Disease, Type C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick Disease, Type C from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Dominant Intermediate C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate C from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 2 from the curated CTD Gene-Disease Associations dataset. |
Pyruvate Dehydrogenase Complex Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Dehydrogenase Complex Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 13 from the curated CTD Gene-Disease Associations dataset. |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L from the curated CTD Gene-Disease Associations dataset. |
Medullary Cystic Kidney Disease 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Medullary Cystic Kidney Disease 2 from the curated CTD Gene-Disease Associations dataset. |
von Willebrand Disease, Type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease von Willebrand Disease, Type 3 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 4C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4C from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 4E Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4E from the curated CTD Gene-Disease Associations dataset. |
Huntington Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Huntington Disease from the curated CTD Gene-Disease Associations dataset. |
PAGET DISEASE, JUVENILE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PAGET DISEASE, JUVENILE from the curated CTD Gene-Disease Associations dataset. |
PARKINSON DISEASE, LATE-ONSET Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE, LATE-ONSET from the curated CTD Gene-Disease Associations dataset. |
Neutral Lipid Storage Disease with Myopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutral Lipid Storage Disease with Myopathy from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Type III Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type III from the curated CTD Gene-Disease Associations dataset. |
End Stage Liver Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease End Stage Liver Disease from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Type II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type II from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 5 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Recessive Intermediate A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Recessive Intermediate A from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 6 from the curated CTD Gene-Disease Associations dataset. |
Hashimoto Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hashimoto Disease from the curated CTD Gene-Disease Associations dataset. |
Canavan Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Canavan Disease from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 1F Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 1F from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2G Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2G from the curated CTD Gene-Disease Associations dataset. |
Krabbe Disease, Atypical, due to Saposin A Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset. |
Stargardt disease 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Stargardt disease 1 from the curated CTD Gene-Disease Associations dataset. |
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease XIII Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease XIII from the curated CTD Gene-Disease Associations dataset. |
Lafora Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lafora Disease from the curated CTD Gene-Disease Associations dataset. |
Van Buchem disease type 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Van Buchem disease type 2 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, X-linked recessive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 3 from the curated CTD Gene-Disease Associations dataset. |
Disease Models, Animal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Disease Models, Animal from the curated CTD Gene-Disease Associations dataset. |
Fabry Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fabry Disease from the curated CTD Gene-Disease Associations dataset. |
Motor Neuron Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Motor Neuron Disease from the curated CTD Gene-Disease Associations dataset. |
Niemann-Pick Disease, Type A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick Disease, Type A from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Type VII Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type VII from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 3 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 5 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 8 from the curated CTD Gene-Disease Associations dataset. |
dowling-degos disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease dowling-degos disease from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 6, Autosomal Recessive Early-Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 6, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset. |
Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset. |
Darier Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Darier Disease from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease from the curated CTD Gene-Disease Associations dataset. |
Paget Disease Of Bone 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Paget Disease Of Bone 4 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2D Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2D from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2E Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2E from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2I from the curated CTD Gene-Disease Associations dataset. |
Disease Progression Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Disease Progression from the curated CTD Gene-Disease Associations dataset. |
Disease Susceptibility Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Disease Susceptibility from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B from the curated CTD Gene-Disease Associations dataset. |
Dent Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dent Disease from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2F Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2F from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2J Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2J from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2H Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2H from the curated CTD Gene-Disease Associations dataset. |
Lewy Body Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lewy Body Disease from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 16 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 16 from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 12 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Axonal, Type 2n Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Axonal, Type 2n from the curated CTD Gene-Disease Associations dataset. |
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset. |
De Vivo disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease De Vivo disease from the curated CTD Gene-Disease Associations dataset. |
Alzheimer disease type 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer disease type 4 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer disease type 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer disease type 2 from the curated CTD Gene-Disease Associations dataset. |
Leigh Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leigh Disease from the curated CTD Gene-Disease Associations dataset. |
Pigmented Nodular Adrenocortical Disease, Primary, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 2 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 28, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 28, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Dominant Intermediate B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Dominant Intermediate B from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease IXC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IXC from the curated CTD Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset. |
AORTIC VALVE DISEASE 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease AORTIC VALVE DISEASE 1 from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Type VI Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type VI from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease IB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IB from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 10 from the curated CTD Gene-Disease Associations dataset. |
Niemann-Pick Disease, Type B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick Disease, Type B from the curated CTD Gene-Disease Associations dataset. |
Raynaud Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Raynaud Disease from the curated CTD Gene-Disease Associations dataset. |
Moyamoya disease 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Moyamoya disease 1 from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Type IIb Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type IIb from the curated CTD Gene-Disease Associations dataset. |
Moyamoya disease 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Moyamoya disease 3 from the curated CTD Gene-Disease Associations dataset. |
Niemann-Pick disease, type C2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Niemann-Pick disease, type C2 from the curated CTD Gene-Disease Associations dataset. |
Hodgkin disease, X-linked pseudoautosomal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hodgkin disease, X-linked pseudoautosomal from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 8 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 9 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 7 from the curated CTD Gene-Disease Associations dataset. |
Sialic Acid Storage Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sialic Acid Storage Disease from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 24 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 24 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease from the curated CTD Gene-Disease Associations dataset. |
Gallbladder Disease 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gallbladder Disease 4 from the curated CTD Gene-Disease Associations dataset. |
Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 20 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 20 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 22 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 22 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 27 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 27 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth Disease, Type 4H Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4H from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 21 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 21 from the curated CTD Gene-Disease Associations dataset. |
Alzheimer Disease 15 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alzheimer Disease 15 from the curated CTD Gene-Disease Associations dataset. |
Inflammatory Bowel Disease 23 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inflammatory Bowel Disease 23 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, X-linked recessive, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, X-linked recessive, 2 from the curated CTD Gene-Disease Associations dataset. |
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset. |
GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease GRAVES DISEASE, SUSCEPTIBILITY TO, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset. |
Peripheral Arterial Occlusive Disease 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Arterial Occlusive Disease 1 from the curated CTD Gene-Disease Associations dataset. |
Maple Syrup Urine Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Maple Syrup Urine Disease from the curated CTD Gene-Disease Associations dataset. |
GLYCOGEN STORAGE DISEASE XV Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease GLYCOGEN STORAGE DISEASE XV from the curated CTD Gene-Disease Associations dataset. |
Gaucher Disease, Type Iiic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Type Iiic from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2B1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B1 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 2B2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 2B2 from the curated CTD Gene-Disease Associations dataset. |
von Hippel-Lindau Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease von Hippel-Lindau Disease from the curated CTD Gene-Disease Associations dataset. |
Multiple Sulfatase Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease from the curated CTD Gene-Disease Associations dataset. |
Graft vs Host Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Graft vs Host Disease from the curated CTD Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 4B1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B1 from the curated CTD Gene-Disease Associations dataset. |
Pelizaeus-Merzbacher Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pelizaeus-Merzbacher Disease from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Type I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type I from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease of Heart, Lethal Congenital Gene SetFrom 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. |
Sandhoff Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sandhoff Disease from the curated CTD Gene-Disease Associations dataset. |
von Willebrand Disease, Type 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease von Willebrand Disease, Type 2 from the curated CTD Gene-Disease Associations dataset. |
von Willebrand Disease, Type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease von Willebrand Disease, Type 1 from the curated CTD Gene-Disease Associations dataset. |
Microvillus inclusion disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microvillus inclusion disease from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 4, Autosomal Dominant Lewy Body Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 4, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease IC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease IC from the curated CTD Gene-Disease Associations dataset. |
Coronary Artery Disease, Autosomal Dominant, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Coronary Artery Disease, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset. |
Desmoid disease, hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Desmoid disease, hereditary from the curated CTD Gene-Disease Associations dataset. |
Pyruvate Carboxylase Deficiency Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyruvate Carboxylase Deficiency Disease from the curated CTD Gene-Disease Associations dataset. |
Gaucher Disease, Perinatal Lethal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Perinatal Lethal from the curated CTD Gene-Disease Associations dataset. |
Gestational Trophoblastic Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gestational Trophoblastic Disease from the curated CTD Gene-Disease Associations dataset. |
Crohn Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Crohn Disease from the curated CTD Gene-Disease Associations dataset. |
Lethal Arthrogryposis With Anterior Horn Cell Disease Gene SetFrom 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. |
PARKINSON DISEASE 11, AUTOSOMAL DOMINANT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PARKINSON DISEASE 11, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset. |
Gerstmann-Straussler-Scheinker Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gerstmann-Straussler-Scheinker Disease from the curated CTD Gene-Disease Associations dataset. |
Dent disease 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dent disease 1 from the curated CTD Gene-Disease Associations dataset. |
Norrie disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Norrie disease from the curated CTD Gene-Disease Associations dataset. |
Rippling muscle disease, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Rippling muscle disease, 1 from the curated CTD Gene-Disease Associations dataset. |
Tay-Sachs Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tay-Sachs Disease from the curated CTD Gene-Disease Associations dataset. |
Charcot-Marie-Tooth disease, Type 4B2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4B2 from the curated CTD Gene-Disease Associations dataset. |
Glycogen Storage Disease Type V Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glycogen Storage Disease Type V from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 7, Autosomal Recessive Early-Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 7, Autosomal Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset. |
Legg-Calve-Perthes Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Legg-Calve-Perthes Disease from the curated CTD Gene-Disease Associations dataset. |
Medullary cystic kidney disease 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Medullary cystic kidney disease 1 from the curated CTD Gene-Disease Associations dataset. |
Celiac Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Celiac Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Coronary Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Coronary Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Hirschsprung Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Hirschsprung Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Gaucher Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Gaucher Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Alzheimer Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Alzheimer Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Non-alcoholic Fatty Liver Disease [Supplementary Concept] Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Non-alcoholic Fatty Liver Disease [Supplementary Concept] in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Hodgkin Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Hodgkin Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Coronary Artery Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Coronary Artery Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Paget's disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Paget's disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Parkinson Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Parkinson Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Moyamoya Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Moyamoya Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Pulmonary Disease, Chronic Obstructive Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Pulmonary Disease, Chronic Obstructive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Crohn Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Crohn Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Nonalcoholic Fatty Liver Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Nonalcoholic Fatty Liver Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Graves Disease Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Graves Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
autoimmune disease of gastrointestinal tract Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease autoimmune disease of gastrointestinal tract from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bronchial disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bronchial disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
collagen disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease collagen disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
diaphragm disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease diaphragm disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
impaired renal function disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease impaired renal function disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone remodeling disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone remodeling disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
polycystic kidney disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease polycystic kidney disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
bone marrow disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bone marrow disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
lafora disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lafora disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |