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peripheral retinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Peripheral Retinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
arterial occlusive diseases; diabetes complications; myocardial infarction; peripheral arterial disease; peripheral arterial diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; diabetes complications; myocardial infarction; peripheral arterial disease; peripheral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral arterial disease; peripheral arterial diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral arterial disease; peripheral arterial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
constriction, pathologic; ischemia; peripheral arterial disease; peripheral arterial diseases; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease constriction, pathologic; ischemia; peripheral arterial disease; peripheral arterial diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral axonal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Peripheral Axonal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
muscular atrophy, spinal; spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
peripheral retinal degeneration Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral retinal pigmentation abnormalities Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral retinal pigmentation abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral retinal avascularization Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral retinal avascularization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral traction retinal detachment Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral traction retinal detachment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Peripheral Retinal Neovascularization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Retinal Degeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Retinal Avascularization Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Retinal Avascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Cystoid Retinal Degeneration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Cystoid Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Tractional Retinal Detachment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Tractional Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral retinal degeneration Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
geographic atrophy; macular degeneration; retinal drusen Gene SetFrom GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
retinal pigment epithelial atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal pigment epithelium atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Retinal Pigment Epithelium Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelium Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Progressive Retinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Retinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Retinal Pigment Epithelial Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Retinal pigment epithelial atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal pigment epithelial atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Retinal atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal neovascularization; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene SetFrom GAD Gene-Disease Associations genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
retinal artery occlusion; retinal vein occlusion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset. |
Retinal detachment or retinal break Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment or retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Retinal detachment with retinal break Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment with retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
peripheral portion of GPi Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in peripheral portion of GPi relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss 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. |
light-harvesting complex, peripheral complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the light-harvesting complex, peripheral complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 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. |
Peripheral Nervous System Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Nervous System Diseases from the curated CTD Gene-Disease Associations dataset. |
Peripheral Vascular Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Vascular Diseases from the curated CTD Gene-Disease Associations dataset. |
Neuroectodermal Tumors, Primitive, Peripheral Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuroectodermal Tumors, Primitive, Peripheral from the curated CTD Gene-Disease Associations dataset. |
Lymphoma, T-Cell, Peripheral Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphoma, T-Cell, Peripheral 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. |
Inherited Peripheral Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inherited Peripheral Neuropathy from the curated CTD Gene-Disease Associations dataset. |
peripheral nervous system neoplasm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease peripheral nervous system neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
peripheral vascular disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease peripheral vascular disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
peripheral primitive neuroectodermal tumor Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease peripheral primitive neuroectodermal tumor from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
peripheral neuropathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease peripheral neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of peripheral nervous system Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease autoimmune disease of peripheral nervous system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
peripheral nervous system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease peripheral nervous system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
peripheral nervous system neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease peripheral nervous system neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
peripheral vascular disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease peripheral vascular disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
peripheral t-cell lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral t-cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
autonomic peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autonomic peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral nervous system neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral nervous system neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral vertigo Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
autoimmune disease of peripheral nervous system Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of peripheral nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral nervous system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral nervous system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sensory peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sensory peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant glandular tumor of peripheral nerve sheath Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant glandular tumor of peripheral nerve sheath in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral vascular disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral nerve sheath neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral nerve sheath neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral osteosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
epithelioid malignant peripheral nerve sheath tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epithelioid malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant peripheral nerve sheath tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
motor peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease motor peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
peripheral primitive neuroectodermal tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral primitive neuroectodermal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; 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. |
peripheral vascular diseases; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral vascular diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; peripheral vascular diseases; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; peripheral vascular diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
calcium homeostasis and peripheral bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease calcium homeostasis and peripheral bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral demyelinating neuropathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral demyelinating neuropathies 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. |
choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
intermittent claudication; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease intermittent claudication; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetic neuropathies; peripheral nervous system diseases; sensation disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetic neuropathies; peripheral nervous system diseases; sensation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy in other diseases; peripheral vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy in other diseases; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; stroke; angina; peripheral vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; stroke; angina; peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; iatrogenic disease; peripheral nervous system diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; iatrogenic disease; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; hypercholesterolemia; hypertension; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; hypercholesterolemia; hypertension; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor vii deficiency; peripheral vascular diseases; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor vii deficiency; peripheral vascular diseases; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral nervous system diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; peripheral vascular diseases 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. |
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. |
colonic neoplasms; peripheral nervous system diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colonic neoplasms; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choroid diseases; macular degeneration; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; peripheral vascular diseases; recurrence; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; peripheral vascular diseases; recurrence; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral vascular diseases; postoperative complications; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral vascular diseases; postoperative complications; thromboembolism 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. |
angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease angina pectoris; ischemic attack, transient; lupus erythematosus, systemic; myocardial infarction; peripheral vascular diseases; stroke; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choroid diseases; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroid diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; intermittent claudication; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; intermittent claudication; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic aneurysm, abdominal; coronary artery disease; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choroid diseases; peripheral vascular diseases; vitreous hemorrhage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroid diseases; peripheral vascular diseases; vitreous hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus; heart failure; myocardial infarction; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; heart failure; myocardial infarction; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
macular degeneration; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperlipidemias; myocardial ischemia; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperlipidemias; myocardial ischemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; hiv infections; peripheral nervous system diseases; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; hiv infections; peripheral nervous system diseases; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral vascular disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apoplexy; myocardial infarction; peripheral vascular diseases; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apoplexy; myocardial infarction; peripheral vascular diseases; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; glomerulonephritis, membranous; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; glomerulonephritis, membranous; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, sickle cell; peripheral vascular diseases; sickle cell anemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, sickle cell; peripheral vascular diseases; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral arterial disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral arterial disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral vascular diseases; systemic scleroderma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease peripheral vascular diseases; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ischemia; peripheral vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ischemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
peripheral Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term peripheral in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Peripheral motor neuropathy_Sciatic Nerve_GSE1947 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Peripheral motor neuropathy_Sciatic Nerve_GSE1947 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
peripheral nervous system axon regeneration Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peripheral nervous system axon regeneration biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of peripheral tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of peripheral tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
peripheral nervous system myelin formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peripheral nervous system myelin formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
myelination in peripheral nervous system Gene SetFrom GO Biological Process Annotations 2015 genes participating in the myelination in peripheral nervous system biological process from the curated GO Biological Process Annotations 2015 dataset. |
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
peripheral nervous system neuron development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peripheral nervous system neuron development biological process from the curated GO Biological Process Annotations 2015 dataset. |
peripheral nervous system neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peripheral nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of peripheral tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of peripheral tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
peripheral nervous system myelin maintenance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peripheral nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2015 dataset. |
peripheral nervous system axon ensheathment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peripheral nervous system axon ensheathment biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of peripheral t cell tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of peripheral t cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of peripheral t cell tolerance induction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of peripheral t cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset. |
peripheral nervous system development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the peripheral nervous system development biological process from the curated GO Biological Process Annotations 2015 dataset. |
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Peripheral artery disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Peripheral artery disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
peripheral vascular disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease peripheral vascular disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
peripheral neuropathy Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease peripheral neuropathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
sensory peripheral neuropathy Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease sensory peripheral neuropathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
peripheral primitive neuroectodermal tumor Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease peripheral primitive neuroectodermal tumor in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
peripheral nervous system neoplasm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease peripheral nervous system neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormalities of the peripheral arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormalities of the peripheral arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
peripheral neuropathy Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the peripheral neuropathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
peripheral primitive neuroectodermal neoplasm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the peripheral primitive neuroectodermal neoplasm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
peripheral arterial disease Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the peripheral arterial disease phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
segmental peripheral demyelination/remyelination Gene SetFrom HPO Gene-Disease Associations genes associated with the segmental peripheral demyelination/remyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symmetrical progressive peripheral demyelination Gene SetFrom HPO Gene-Disease Associations genes associated with the symmetrical progressive peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature peripheral vascular disease Gene SetFrom HPO Gene-Disease Associations genes associated with the premature peripheral vascular disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral vitreoretinal degeneration Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral vitreoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral axonal neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged peripheral nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged peripheral nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral retinopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral retinopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral pulmonary artery stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral pulmonary artery stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral schwannoma Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral schwannoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral dysmyelination Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral dysmyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased number of small peripheral myelinated nerve fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral primitive neuroectodermal neoplasm Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral primitive neuroectodermal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
demyelinating peripheral neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the demyelinating peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased number of large peripheral myelinated nerve fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased number of large peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral arteriovenous fistula Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral arteriovenous fistula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral nerve compression Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive peripheral neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent microvilli on the surface of peripheral blood lymphocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the absent microvilli on the surface of peripheral blood lymphocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral hypermyelination Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral hypermyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
delayed peripheral myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the delayed peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormalities of the peripheral arteries Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormalities of the peripheral arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral hypomyelination Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral hypomyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic peripheral neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral pulmonary vessel aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral pulmonary vessel aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral vitreous opacities Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral vitreous opacities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral axonal degeneration Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral axonal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral arterial stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral arterial stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased number of peripheral cd3+ t cells Gene SetFrom HPO Gene-Disease Associations genes associated with the increased number of peripheral cd3+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
segmental peripheral demyelination Gene SetFrom HPO Gene-Disease Associations genes associated with the segmental peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased number of peripheral myelinated nerve fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased number of peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral opacification of the cornea Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral visual field loss Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral visual field loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral demyelination Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal peripheral sensory neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symmetric peripheral demyelination Gene SetFrom HPO Gene-Disease Associations genes associated with the symmetric peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the peripheral nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the peripheral nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerve conduction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerve conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral vascular insufficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral vascular insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neovascularization of peripheral and posterior retina Gene SetFrom HPO Gene-Disease Associations genes associated with the neovascularization of peripheral and posterior retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral arterial disease Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral arterial disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral action potential amplitude Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Peripheral Nervous System Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Peripheral Nervous System Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Peripheral Vascular Diseases Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Peripheral Vascular Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lymphoma, T-Cell, Peripheral Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lymphoma, T-Cell, Peripheral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Peripheral Arterial Disease Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Peripheral Arterial Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Peripheral myelin protein PMP22 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peripheral myelin protein PMP22 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal peripheral nervous system regeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal peripheral nervous system regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal peripheral b cell anergy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal peripheral b cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal peripheral t cell anergy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal peripheral t cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal peripheral lymph node morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal peripheral lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent peripheral lymph nodes Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent peripheral lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
peripheral nervous system degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the peripheral nervous system degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
peripheral arterial occlusive disease 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the peripheral arterial occlusive disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
agenesis of the corpus callosum with peripheral neuropathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the agenesis of the corpus callosum with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
deafness, autosomal dominant, with peripheral neuropathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant, with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
peripheral blood mononuclear cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral blood mononuclear cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
peripheral ganglion Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral ganglion from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
peripheral blood Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral blood from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
peripheral blood lymphocyte Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral blood lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
peripheral nerve Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral nerve from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
peripheral nervous system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral nervous system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
peripheral ganglion Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
peripheral nervous system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral nervous system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
peripheral blood Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue peripheral blood in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
peripheral primitive neuroectodermal tumor cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral primitive neuroectodermal tumor cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
malignant peripheral nerve sheath cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue malignant peripheral nerve sheath cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral blood mononuclear cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral blood mononuclear cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral blood stem cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral blood stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral blood Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral blood in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral blood cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral blood cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral nerve Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral blood lymphocyte Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral blood lymphocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral nerve sheath cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral nerve sheath cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
peripheral nervous system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue peripheral nervous system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Peripheral Axonal Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Arterial Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Arterial Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Neuroepithelioma Of Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuroepithelioma Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Neuropathy Due To And Following Chemotherapy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuropathy Due To And Following Chemotherapy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Demyelinating Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Arterial Occlusive Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Arterial Occlusive Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Arteriovenous Fistula Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Arteriovenous Fistula in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral T-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Arthritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Arthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Arterial Calcification Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Arterial Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Vascular Insufficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Vascular Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Nerve Sheath Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Nerve Sheath Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Unspecified Idiopathic Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Unspecified Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Neoplastic Peripheral Nervous System Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Neoplastic Peripheral Nervous System Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Schwannoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Schwannoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Peripheral Nervous System Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Peripheral Nervous System Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Artery Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neuroepithelioma, Peripheral Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neuroepithelioma, Peripheral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Pulmonary Artery Stenosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Pulmonary Artery Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Peripheral Chondrosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Peripheral Chondrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epithelioid Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epithelioid Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Ameloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Ameloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Low Grade Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Low Grade Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Nerve Lesion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Nerve Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metastatic Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous/Peripheral T-Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous/Peripheral T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Length-Dependent Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Length-Dependent Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Anterior Synechiae Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Anterior Synechiae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Peripheral Myelination Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Peripheral Myelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Peripheral Sensory Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Peripheral Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inherited Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inherited Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Artery Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Artery Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Precocious Puberty Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Symmetrical Progressive Peripheral Demyelination Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Symmetrical Progressive Peripheral Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Arteriosclerosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Arteriosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hiv Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hiv Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Spondyloarthritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Spondyloarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Lymphadenopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Lymphadenopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Obsolete Peripheral Retinopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Obsolete Peripheral Retinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Ulcerative Keratitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Ulcerative Keratitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Symmetric Peripheral Demyelination Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Symmetric Peripheral Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Angiopathy In Diseases Classified Elsewhere Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Angiopathy In Diseases Classified Elsewhere in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bone Surface (Peripheral) Osteosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bone Surface (Peripheral) Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Peripheral Nerve Sheath Tumor With Rhabdomyoblastic Differentiation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Peripheral Nerve Sheath Tumor With Rhabdomyoblastic Differentiation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Dysostosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Dysostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Cone Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Amyelination Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Amyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Ossifying Fibroma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Ossifying Fibroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Resistance To Thyroid Hormone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Resistance To Thyroid Hormone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ischemic Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripheral Demyelination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Neuropathic Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Neuropathic Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Visual Field Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Visual Field Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Number Of Large Peripheral Myelinated Nerve Fibers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Number Of Large Peripheral Myelinated Nerve Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Axonal Degeneration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Axonal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Peripheral Myelination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Peripheral Myelination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Segmental Peripheral Demyelination/Remyelination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Segmental Peripheral Demyelination/Remyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Peripheral Nerve Conduction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Peripheral Nerve Conduction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Hypomyelination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Hypomyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Number Of Peripheral Myelinated Nerve Fibers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Number Of Peripheral Myelinated Nerve Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Dysmyelination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Dysmyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Nerve Compression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Nerve Compression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Peripheral Neuropathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Edema Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Neuropathy With Sensorineural Hearing Impairment Syndrome Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Neuropathy With Sensorineural Hearing Impairment Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Enlarged Peripheral Nerve Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlarged Peripheral Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Opacity Of Cornea Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Opacity Of Cornea in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Vitreous Opacities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Vitreous Opacities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Number Of Small Peripheral Myelinated Nerve Fibers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Number Of Small Peripheral Myelinated Nerve Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Vitreoretinal Degeneration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Vitreoretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Segmental Peripheral Demyelination Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Segmental Peripheral Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Neuralgia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Neuralgia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Microvilli On The Surface Of Peripheral Blood Lymphocytes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Microvilli On The Surface Of Peripheral Blood Lymphocytes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Pulmonary Vessel Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Pulmonary Vessel Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
peripheral nervous system development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral nervous system development biological process from the curated GO Biological Process Annotations 2023 dataset. |
myelination in peripheral nervous system Gene SetFrom GO Biological Process Annotations 2023 genes participating in the myelination in peripheral nervous system biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral T cell tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral T cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral nervous system myelin maintenance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral nervous system axon regeneration Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral nervous system axon regeneration biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral nervous system neuron development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral nervous system neuron development biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral nervous system neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral nervous system myelin formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral nervous system myelin formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral nervous system axon ensheathment Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral nervous system axon ensheathment biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
peripheral nervous system neuron differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the peripheral nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of peripheral tolerance induction Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of peripheral tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal peripheral nervous system regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal peripheral nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed peripheral nervous system regeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed peripheral nervous system regeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent peripheral lymph nodes Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent peripheral lymph nodes phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal peripheral lymph node morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal peripheral lymph node morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
peripheral nervous system degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the peripheral nervous system degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal peripheral T cell anergy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal peripheral T cell anergy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal peripheral B cell anergy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal peripheral B cell anergy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Peripheral immune cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Peripheral immune cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Activated peripheral helper T cell_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Activated peripheral helper T cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Peripheral blood mononuclear cell (PBMC)_Blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Peripheral blood mononuclear cell (PBMC)_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Peripheral blood mononuclear cell (PBMC)_Peripheral blood_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Peripheral blood mononuclear cell (PBMC)_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
T peripheral helper(Tph) cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the T peripheral helper(Tph) cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Pathogenic T peripheral helper cell_Salivary gland_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pathogenic T peripheral helper cell_Salivary gland_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Thyroid hormones production and peripheral downstream signaling effects Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Thyroid hormones production and peripheral downstream signaling effects pathway from the WikiPathways Pathways 2024 dataset. |
Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) Gene Setproteins participating in the Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) pathway from the Reactome Pathways 2024 dataset. |
Peripheral nervous system_CT1_neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT1_neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT2_schwann cell Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT2_schwann cell cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_intrinsic cardiac ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_intrinsic cardiac ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_superior cervical ganglion TH/DBH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion TH/DBH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_superior cervical ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_superior cervical ganglion NPY neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion NPY neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_superior cervical ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_superior cervical ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_superior cervical ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion CGRP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_middle cervical ganglion DBH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion DBH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_middle cervical ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_middle cervical ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_middle cervical ganglion NPY neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion NPY neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_middle cervical ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervicothoracic ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervicothoracic ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervicothoracic ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervicothoracic ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervicothoracic ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervicothoracic ganglion VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar ganglion SST/TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion SST/TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar ganglion NPY neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion NPY neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_sacral ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_sacral ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_celiac ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_celiac ganglion VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_celiac ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_celiac ganglion CGRP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_celiac ganglion SOM/CGRP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_celiac ganglion SOM/CGRP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_inferior mesenteric ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_inferior mesenteric ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_otic ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_otic ganglion nNOS neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_otic ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_otic ganglion VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_ciliary ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_ciliary ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_submandibular ganglion TH cholinergic neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_submandibular ganglion TH cholinergic neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_submandibular ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_submandibular ganglion nNOS neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_pterygopalatine ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_pterygopalatine ganglion VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_pterygopalatine ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_pterygopalatine ganglion nNOS neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_ovarian nerve plexus ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_ovarian nerve plexus ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion Nav1.7 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion Nav1.7 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion Peripherin neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion Peripherin neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion BRN3A neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion BRN3A neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion Piezo2 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion Piezo2 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion CGRP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion Endothelin 1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion Endothelin 1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion Nav1.7 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion Nav1.7 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion Peripherin neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion Peripherin neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion BRN3A neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion BRN3A neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion Piezo2 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion Piezo2 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion CGRP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion Endothelin 1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion Endothelin 1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion Nav1.7 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion Nav1.7 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion Peripherin neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion Peripherin neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion BRN3A neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion BRN3A neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion Piezo2 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion Piezo2 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion CGRP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion Endothelin 1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion Endothelin 1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion Nav1.7 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion Nav1.7 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion Peripherin neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion Peripherin neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion BRN3A neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion BRN3A neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion Piezo2 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion Piezo2 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion CGRP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion Endothelin 1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion Endothelin 1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_nodose ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_nodose ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_nodose ganglion P2X3 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_nodose ganglion P2X3 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_nodose ganglion TRPV2 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_nodose ganglion TRPV2 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_nodose ganglion PVALB neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_nodose ganglion PVALB neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_jugular ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_jugular ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_jugular ganglion TRPV2 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_jugular ganglion TRPV2 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_jugular ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_jugular ganglion CGRP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_jugular ganglion SPARCL1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_jugular ganglion SPARCL1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_geniculate ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_geniculate ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_geniculate ganglion SPARCL1 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_geniculate ganglion SPARCL1 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT4_geniculate ganglion VGLUT2 neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT4_geniculate ganglion VGLUT2 neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_myenteric ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_myenteric ganglion nNOS neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_myenteric ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_myenteric ganglion VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_pelvic ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion TH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_pelvic ganglion TH/DBH neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion TH/DBH neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_pelvic ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion nNOS neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_pelvic ganglion nNOS/VIP neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion nNOS/VIP neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_pelvic ganglion NPY/VAChT neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion NPY/VAChT neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT3_pelvic ganglion nNOS/VAChT neuron Gene SetFrom HuBMAP ASCT+B Annotations biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion nNOS/VAChT neuron cell type from the HuBMAP ASCT+B dataset. |
Peripheral nervous system_CT1_neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT1_neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT2_schwann cell Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT2_schwann cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_ciliary ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_ciliary ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_lower airway ganglion ChAT/VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_myenteric ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_myenteric ganglion VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_myenteric ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_myenteric ganglion nNOS neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_otic ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_otic ganglion VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_otic ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_otic ganglion nNOS neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_ovarian nerve plexus ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_ovarian nerve plexus ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_pelvic ganglion NPY/VAChT neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion NPY/VAChT neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_pelvic ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_pelvic ganglion TH/DBH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion TH/DBH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_pelvic ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion nNOS neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_pelvic ganglion nNOS/VAChT neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion nNOS/VAChT neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_pelvic ganglion nNOS/VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_pelvic ganglion nNOS/VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_pterygopalatine ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_pterygopalatine ganglion VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_pterygopalatine ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_pterygopalatine ganglion nNOS neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_submandibular ganglion TH cholinergic neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_submandibular ganglion TH cholinergic neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT3_submandibular ganglion nNOS neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT3_submandibular ganglion nNOS neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_celiac ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_celiac ganglion CGRP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_celiac ganglion SOM/CGRP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_celiac ganglion SOM/CGRP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_celiac ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_celiac ganglion VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion BRN3A neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion BRN3A neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion CGRP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion Endothelin 1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion Endothelin 1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion Nav1.7 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion Nav1.7 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion Peripherin neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion Peripherin neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion Piezo2 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion Piezo2 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervical dorsal root ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervical dorsal root ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervicothoracic ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervicothoracic ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervicothoracic ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervicothoracic ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_cervicothoracic ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_cervicothoracic ganglion VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_geniculate ganglion SPARCL1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_geniculate ganglion SPARCL1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_geniculate ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_geniculate ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_geniculate ganglion VGLUT2 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_geniculate ganglion VGLUT2 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_inferior mesenteric ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_inferior mesenteric ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_intrinsic cardiac ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_intrinsic cardiac ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_jugular ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_jugular ganglion CGRP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_jugular ganglion SPARCL1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_jugular ganglion SPARCL1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_jugular ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_jugular ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_jugular ganglion TRPV2 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_jugular ganglion TRPV2 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion BRN3A neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion BRN3A neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion CGRP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion Endothelin 1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion Endothelin 1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion Nav1.7 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion Nav1.7 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion Peripherin neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion Peripherin neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion Piezo2 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion Piezo2 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar dorsal root ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar dorsal root ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar ganglion NPY neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion NPY neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar ganglion SST/TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion SST/TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_lumbar ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_lumbar ganglion VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_middle cervical ganglion DBH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion DBH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_middle cervical ganglion NPY neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion NPY neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_middle cervical ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_middle cervical ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_middle cervical ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_middle cervical ganglion VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_nodose ganglion P2X3 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_nodose ganglion P2X3 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_nodose ganglion PVALB neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_nodose ganglion PVALB neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_nodose ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_nodose ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_nodose ganglion TRPV2 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_nodose ganglion TRPV2 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion BRN3A neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion BRN3A neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion CGRP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion Endothelin 1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion Endothelin 1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion Nav1.7 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion Nav1.7 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion Peripherin neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion Peripherin neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion Piezo2 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion Piezo2 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_sacral dorsal root ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_sacral dorsal root ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_sacral ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_sacral ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_superior cervical ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion CGRP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_superior cervical ganglion NPY neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion NPY neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_superior cervical ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_superior cervical ganglion TH/DBH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion TH/DBH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_superior cervical ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_superior cervical ganglion VIP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_superior cervical ganglion VIP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion BRN3A neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion BRN3A neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion CGRP neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion CGRP neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion Endothelin 1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion Endothelin 1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion Nav1.7 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion Nav1.7 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion Peripherin neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion Peripherin neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion Piezo2 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion Piezo2 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic dorsal root ganglion TRPV1 neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic dorsal root ganglion TRPV1 neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic ganglion TH neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic ganglion TH neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
Peripheral nervous system_CT4_thoracic ganglion TH/NPY neuron Gene SetFrom HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Peripheral nervous system_CT4_thoracic ganglion TH/NPY neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset. |
peripheral nervous system development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral nervous system development biological process from the curated GO Biological Process Annotations 2025 dataset. |
myelination in peripheral nervous system Gene SetFrom GO Biological Process Annotations 2025 genes participating in the myelination in peripheral nervous system biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral T cell tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral T cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral nervous system myelin maintenance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral nervous system myelin maintenance biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral nervous system axon regeneration Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral nervous system axon regeneration biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral B cell tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral nervous system neuron development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral nervous system neuron development biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral nervous system neuron axonogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral nervous system neuron axonogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral nervous system myelin formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral nervous system myelin formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral nervous system axon ensheathment Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral nervous system axon ensheathment biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral tolerance induction Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset. |
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
peripheral nervous system neuron differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the peripheral nervous system neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Peripheral T-cell lymphoma Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Peripheral T-cell lymphoma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Peripheral nervous system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Peripheral nervous system disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autoimmune disease of peripheral nervous system Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autoimmune disease of peripheral nervous system from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Peripheral nervous system neoplasm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Peripheral nervous system neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Agenesis of the corpus callosum with peripheral neuropathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Agenesis of the corpus callosum with peripheral neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Peripheral artery disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Peripheral artery disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune disease of peripheral nervous system Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autoimmune disease of peripheral nervous system in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral nervous system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Peripheral nervous system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral nervous system neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Peripheral nervous system neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral nervous system neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral nervous system neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral nervous system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral nervous system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral T-cell lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral T-cell lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral vascular disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral vascular disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral nerve sheath neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral nerve sheath neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Motor peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Motor peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral vertigo Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral vertigo in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune disease of peripheral nervous system Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune disease of peripheral nervous system in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral artery disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral artery disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sensory peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensory peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant peripheral nerve sheath tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral osteosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autoimmune peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral nervous system benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral nervous system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autonomic peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autonomic peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Epithelioid malignant peripheral nerve sheath tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelioid malignant peripheral nerve sheath tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Agenesis of the corpus callosum with peripheral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Agenesis of the corpus callosum with peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Idiopathic peripheral autonomic neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic peripheral autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant glandular tumor of peripheral nerve sheath Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant glandular tumor of peripheral nerve sheath in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral nerve schwannoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral nerve schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Malignant melanocytic neoplasm of the peripheral nerve sheath Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant melanocytic neoplasm of the peripheral nerve sheath in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Peripheral nervous system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral nervous system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral blood from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood lymphocyte Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral blood lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood mononuclear cell Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral blood mononuclear cell from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral ganglion Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral ganglion from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral nerve Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral nerve from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral ganglion Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral blood in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral nervous system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Peripheral nervous system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral blood in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood mononuclear cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral blood mononuclear cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood stem cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral blood stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral nerve Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral nervous system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral nervous system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral ganglion Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral blood cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral blood lymphocyte Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral blood lymphocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Malignant peripheral nerve sheath cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Malignant peripheral nerve sheath cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral nerve sheath cancer cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral nerve sheath cancer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Peripheral primitive neuroectodermal tumor cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Peripheral primitive neuroectodermal tumor cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
light-harvesting complex, peripheral complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the light-harvesting complex, peripheral complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Peripheral region of growth cone Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Peripheral region of growth cone cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Peripheral axonal neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SCN9A-related peripheral neuropathies associated Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN9A-related peripheral neuropathies associated phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral visual field loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral visual field loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral demyelination Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral demyelination phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Demyelinating peripheral neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Demyelinating peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Familial dilated cardiomyopathy and peripheral neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial dilated cardiomyopathy and peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral schwannoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral schwannoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary peripheral neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive peripheral neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral motor neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Peripheral arterial disease x type 2 diabetes interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peripheral arterial disease x type 2 diabetes interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bortezomib-induced peripheral neuropathy in multiple myeloma Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bortezomib-induced peripheral neuropathy in multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Peripheral arterial disease (traffic-related air pollution interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peripheral arterial disease (traffic-related air pollution interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diabetic peripheral neuropathy in type 2 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic peripheral neuropathy in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Peripheral artery disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peripheral artery disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Taxane-induced peripheral neuropathy in breast cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Taxane-induced peripheral neuropathy in breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Peripheral artery disease (borderline) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Peripheral artery disease (borderline) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bosch-boonstra-schaaf optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dominant hereditary optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, type II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, X-linked 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked myopathy with postural muscle atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic Atrophy Type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital microvillous atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, autosomal recessive 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sveinsson Chorioretinal Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sveinsson Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy, Jerash type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 1 and deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 5 from the curated CTD Gene-Disease Associations dataset. |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Spinal muscular atrophy with respiratory distress 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset. |
Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Atrophy from the curated CTD Gene-Disease Associations dataset. |
Muscular Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy from the curated CTD Gene-Disease Associations dataset. |
Myopathy, X-Linked, With Postural Muscle Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset. |
Costeff optic atrophy syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy polyneuropathy deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Chorioretinal atrophy, progressive bifocal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset. |
Optic atrophy and cataract, autosomal dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
Gyrate Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gyrate Atrophy from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset. |
Pigmented Paravenous Chorioretinal Atrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset. |
OPTIC ATROPHY 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease OPTIC ATROPHY 2 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset. |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Muscular Atrophy, Spinal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset. |
spinal muscular atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
dentatorubral-pallidoluysian atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
multiple system atrophy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
adult spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atrophy of prostate Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
juvenile spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
intermediate spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
skin atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
atrophy of testis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
multiple system atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary choroidal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dentatorubral-pallidoluysian atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
partial optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
progressive muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
olivopontocerebellar atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
survival motor neuron spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gyrate atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
choroidal neovascularization; geographic atrophy; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; dementia; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; helicobacter infections; metaplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choroidal neovascularization; geographic atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
posterior cortical atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease posterior cortical atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
geographic atrophy; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; helicobacter infections; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; helicobacter infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; prenatal exposure delayed effects; substance-related disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; prenatal exposure delayed effects; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic disc atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic disc atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gyrate atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gyrate atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dementia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; peptic ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; peptic ulcer 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. |
blindness; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; choroidal neovascularization; macular degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; gastritis; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
muscular atrophy, spinal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy; dementia; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; memory disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; aphasia; atrophy; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; aphasia; atrophy; syndrome 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. |
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. |
spinal muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; multiple sclerosis, relapsing-remitting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gastric atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastric atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal muscular atrophy phenotype Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy, hereditary, leber; vision disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; amnesia; atrophy; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; amnesia; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stomach cancer; stomach atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stomach cancer; stomach atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcoholism; atrophy; brain diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcoholism; atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; epilepsy; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophy and moderate deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophy and moderate deafness 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. |
atrophy; gastritis; helicobacter infections; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; stomach neoplasms 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. |
schizophrenia; brain atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease schizophrenia; brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy; huntington disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrophy; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hippocampal atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hippocampal atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dystonic disorders; multiple system atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrophy Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term atrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
skeletal muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
striated muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
muscle atrophy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset. |
MRI atrophy measures Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the MRI atrophy measures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hippocampal atrophy Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hippocampal atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
muscular atrophy Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease muscular atrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
motor neuron atrophy Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the motor neuron atrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
atrophy/degeneration affecting the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
type 2 muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the type 2 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
levator palpebrae superioris atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the levator palpebrae superioris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral white matter atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration involving the corticospinal tracts Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized limb muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
global brain atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the global brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
caudate atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the caudate atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corpus callosum atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the corpus callosum atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the tubular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thenar muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the thenar muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pontocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse cerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
brain atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skeletal muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the skeletal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tongue atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the tongue atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
olivopontocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the olivopontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dermal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the dermal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripapillary chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the frontal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
subcortical cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse skin atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hand muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
motor neuron atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pelvic girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pelvic girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
leber optic atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fundus atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the fundus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scapular muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the scapular muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the cerebrum Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
first dorsal interossei muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the first dorsal interossei muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nonprogressive muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration affecting the brainstem Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration involving the caudate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the caudate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic atrophy from cranial nerve compression Gene SetFrom HPO Gene-Disease Associations genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar vermis atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
villous atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the villous atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
iris atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the iris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the renal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
interosseus muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the interosseus muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy/degeneration involving the spinal cord Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
type 1 muscle fiber atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
superior rectus atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the superior rectus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
noninflammatory macular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the noninflammatory macular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized cerebral atrophy/hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diffuse cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
limb-girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the limb-girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
testicular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the testicular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shoulder girdle muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the shoulder girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pigmented paravenous chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peroneal muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the peroneal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of the spinal cord Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chorioretinal atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontotemporal cerebral atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the frontotemporal cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atrophy of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the atrophy of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
quadriceps muscle atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the quadriceps muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinocerebellar atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the spinocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
temporal cortical atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the temporal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Multiple System Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy, Autosomal Dominant Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Muscular Atrophy, Spinal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Muscular Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Geographic Atrophy Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Geographic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Optic atrophy 3-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
dentatorubropallidoluysian atrophy Gene SetFrom KEGG Pathways proteins participating in the dentatorubropallidoluysian atrophy pathway from the KEGG Pathways dataset. |
ovary atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ovary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle fiber atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney cortex atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
testicular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the testicular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney collecting duct atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thymus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thymus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
brain atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the brain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
skeletal muscle atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
optic nerve atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
sebaceous gland atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
midbrain atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal tubule atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
seminal vesicle atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
renal glomerulus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
meibomian gland atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the meibomian gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
uterus atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreatic acinar cell atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
endometrium atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epidermal atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the epidermal atrophy 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. |
spleen atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the spleen atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
iris atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the iris atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vagina atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vagina atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased susceptibility to induced muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased susceptibility to induced muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
vulva atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vulva atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
muscular atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the muscular atrophy 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. |
oviduct atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
external male genitalia atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney medulla atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
kidney papillary atrophy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy-4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, postnatal progressive, with seizures and brain atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy with progressive myoclonic epilepsy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, x-linked 2, infantile Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy-4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{multiple system atrophy, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, x-linked, with postural muscle atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, chronic distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, jokela type Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset. |
sveinsson choreoretinal atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the sveinsson choreoretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
scapuloperoneal spinal muscular atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, late-onset, finkel type Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset. |
dentatorubro-pallidoluysian atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the dentatorubro-pallidoluysian atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
{spinal muscular atrophy, type iii, modifier of} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy-7 Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, lower extremity-predominant 1, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
spastic paraplegia, optic atrophy, and neuropathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
bosch-boonstra-schaaf optic atrophy syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 2, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
gyrate atrophy of choroid and retina with or without ornithinemia Gene SetFrom OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy 3 with cataract Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, lower extremity-predominant, 2, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcornea, myopic chorioretinal atrophy, and telecanthus Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, x-linked 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
short stature, optic nerve atrophy, and pelger-huet anomaly Gene SetFrom OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset. |
pigmented paravenous chorioretinal atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neurodegeneration with optic atrophy, childhood onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal and bulbar muscular atrophy of kennedy Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset. |
optic atrophy plus syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the optic atrophy plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, congenital nonprogressive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset. |
{leber optic atrophy, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Geographic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Geographic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bulbo-Spinal Atrophy, X-Linked Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bulbo-Spinal Atrophy, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chorioretinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Linear Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Linear Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brain Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Testis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Testis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Olivopontocerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Infantile Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Limb Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Limb Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscle Fiber Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple System Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Motor Neuron Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Subcortical Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Subcortical Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sveinsson Chorioretinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sveinsson Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Kidney Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Villous Atrophy Of Intestine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Villous Atrophy Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontotemporal Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Cerebral Atrophy/Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Cerebral Atrophy/Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dentatorubral-Pallidoluysian Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dentatorubral-Pallidoluysian Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy, Disuse Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Disuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of The Spinal Cord Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Corpus Callosum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral White Matter Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral White Matter Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Prostate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pelvic Girdle Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pelvic Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy, Muscular, Spinobulbar Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Muscular, Spinobulbar in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proliferative Inflammatory Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proliferative Inflammatory Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gyrate Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Distal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy/Degeneration Affecting The Brainstem Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy/Degeneration Affecting The Brainstem in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple System Atrophy, Cerebellar Variant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Optic Disc Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebellar Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dominant Hereditary Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dominant Hereditary Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Liver Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Atrophy Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Atrophy Of Ovary 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. |
Atrophy Of Tongue Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paravenous Chorioretinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pigmented Paravenous Chorioretinal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pigmented Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Limb-Girdle Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Cortical Atrophy Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Cortical Atrophy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Vagina Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Urogenital Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Urogenital Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peroneal Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Juvenile Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chorioretinal Atrophy, Progressive Bifocal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy, Progressive Bifocal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Auditory Neuropathy And Optic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Skin Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Skin Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervical Spinal Cord Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervical Spinal Cord Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Splenic Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Splenic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Atrophy Of Thyroid Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atrophy Of Thyroid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sporadic Olivopontocerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sporadic Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Tongue Papillae Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue Papillae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pancreatic Acinar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pancreatic Acinar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Tubular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glaucomatous Atrophy Of Optic Disc Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Leber Optic Atrophy And Dystonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Leber Optic Atrophy And Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Atrophy Of Seminal Vesicle Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Seminal Vesicle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peripapillary Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Dominant Optic Atrophy Plus Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Optic Atrophy Plus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Late Cortical Cerebellar Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Late Cortical Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rectus Femoris Muscle Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rectus Femoris Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Parietal Cortical Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Parietal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myelopathic Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oculopharyngeal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngeal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Proximal Myelopathic Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Scapuloperoneal Form Of Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Form Of Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Recessive Cerebral Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonprogressive Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodontal Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Skeletal Muscle Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skeletal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Foveal Atrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foveal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |