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alveolar bone loss; chronic periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontal attachment loss; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontitis; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; chronic periodontitis; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; chronic periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontal attachment loss; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; gram-negative bacterial infections; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; gram-negative bacterial infections; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; dental fistula; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; dental fistula; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; periodontitis; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; dental caries; periodontitis; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; dental caries; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss; periodontal attachment loss; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; chronic periodontitis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; chronic periodontitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; chronic periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; chronic periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic periodontitis; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic periodontitis; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; bone resorption; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; bone resorption; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic periodontitis; periodontal attachment loss; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complete hearing loss; deafness; hearing loss, sensorineural; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Alveolar Bone Loss Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alveolar Bone Loss from the curated CTD Gene-Disease Associations dataset. |
alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar bone loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Alveolar Bone Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Alveolar Bone Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Alveolar Bone Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alveolar Bone Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alveolar Bone Loss Around Teeth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alveolar Bone Loss Around Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
aggressive periodontitis; periodontitis, juvenile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
low bone-mineral density and rapid postmenopausal bone loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease low bone-mineral density and rapid postmenopausal bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periodontal attachment loss; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periodontal attachment loss; periodontitis; tooth mobility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; periodontal attachment loss; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha 1-antitrypsin deficiency; bronchitis, chronic; chronic bronchitis ; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholangitis, sclerosing; fatty liver; hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune; hepatitis, chronic; liver cirrhosis, alcoholic; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Chronic Periodontitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chronic Periodontitis from the curated CTD Gene-Disease Associations dataset. |
chronic apical periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic apical periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic periodontitis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic periodontitis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic periodontitis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic periodontitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic periodontitis; diabetes complications; diabetes mellitus, type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic periodontitis; diabetes complications; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney failure, chronic; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney failure, chronic; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Chronic periodontitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Chronic periodontitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Chronic Periodontitis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Chronic Periodontitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Chronic Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Chronic Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Chronic Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Localized Chronic Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Localized Chronic Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic apical periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic apical periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chronic periodontitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic periodontitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic periodontitis (localised) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic periodontitis (localised) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic periodontitis (mean interproximal clinical attachment level) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic periodontitis (mean interproximal clinical attachment level) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
hearing loss; hearing loss, sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; sensorineural hearing loss; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; sensorineural hearing loss; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complete hearing loss; deafness; hearing loss, bilateral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing loss, bilateral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; hemoglobin sc disease; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; hemoglobin sc disease; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; hearing loss, high-frequency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, high-frequency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, bilateral; hearing loss, sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, bilateral; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
deafness; hearing loss; hearing loss, sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease deafness; hearing loss; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal loss, late; pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal loss, late; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; hearing loss, sudden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complete hearing loss; deafness; hearing impairment; hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Loss of function of TP53 in cancer due to loss of tetramerization ability Gene Setproteins participating in the Loss of function of TP53 in cancer due to loss of tetramerization ability pathway from the Reactome Pathways 2024 dataset. |
alveolar bone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar bone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Alveolar bone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar bone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
hip bone loss and fracture Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hip bone loss and fracture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone neoplasms; hearing loss; osteosarcoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone neoplasms; hearing loss; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early postmenopausal bone loss at the spine. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early postmenopausal bone loss at the spine. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early marginal bone loss around endosseous dental implants. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early marginal bone loss around endosseous dental implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early marginal bone loss around endosseous implants. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early marginal bone loss around endosseous implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Periapical Bone Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Periapical Bone Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
chronic renal failure; diabetes mellitus; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; nephrosclerosis; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; hypertension; nephrosclerosis; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension; nephrosclerosis; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; chronic b-cell leukemias; leukemia, lymphocytic, chronic, b-cell; lupus erythematosus, systemic; mammary neoplasms; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; chronic b-cell leukemias; leukemia, lymphocytic, chronic, b-cell; lupus erythematosus, systemic; mammary neoplasms; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; nephritis, interstitial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; nephritis, interstitial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; inflammation; kidney failure, chronic; wasting syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; inflammation; kidney failure, chronic; wasting syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; chronic renal failure; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; lipoid nephrosis; nephrosis, lipoid Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; lipoid nephrosis; nephrosis, lipoid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; calcinosis; cardiovascular diseases; chronic renal failure; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; calcinosis; cardiovascular diseases; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b, chronic; hepatitis c, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b, chronic; hepatitis c, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypercalcemia; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypercalcemia; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bronchitis, chronic; bronchopneumonia; chronic bronchitis ; communicable diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bronchitis, chronic; bronchopneumonia; chronic bronchitis ; communicable diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dna damage; leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dna damage; leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
african trypanosomiasis, unspecified; chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney failure, chronic; trypanosomiasis, african Gene SetFrom GAD Gene-Disease Associations genes associated with the disease african trypanosomiasis, unspecified; chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; hypertension; kidney failure, chronic; trypanosomiasis, african in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic b-cell leukemias; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic b-cell leukemias; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; vasculitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hyperhomocysteinemia; kidney failure, chronic; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hyperhomocysteinemia; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; inflammation; kidney failure, chronic; malnutrition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; inflammation; kidney failure, chronic; malnutrition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; nephrotic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; gout; kidney calculi; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; gout; kidney calculi; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b, chronic; hepatitis c, chronic; liver cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b, chronic; hepatitis c, chronic; liver cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadaver; chronic renal failure; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadaver; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; uremia; vesico-ureteral reflux; vesicoureteral reflux Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; uremia; vesico-ureteral reflux; vesicoureteral reflux in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus; endocrine system diseases; kidney failure, chronic; urologic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus; endocrine system diseases; kidney failure, chronic; urologic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; myocardial infarction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus; glomerulonephritis; kidney failure, chronic; nephrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus; glomerulonephritis; kidney failure, chronic; nephrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hemochromatosis; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hemochromatosis; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney diseases; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney diseases; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension; kidney failure, chronic; nephrosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; nephrosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; inflammation; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; inflammation; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; chronic renal failure; inflammation; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; chronic renal failure; inflammation; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; fibrosis; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; nephritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; nephritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; diabetic retinopathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd; 21-hydroxylase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brill-symmers disease; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; lymphoma, follicular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brill-symmers disease; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; lymphoma, follicular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; chronic bronchopulmonary diseases; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; lymphoma; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; lymphoma; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; nephrotic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic; nephrotic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetic nephropathies; diabetic nephropathy; glomerulonephritis; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetic nephropathies; diabetic nephropathy; glomerulonephritis; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; chronic renal failure; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; lcc - liver cell carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; hypertension, renal; proteinuria; renal hypertension; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b, chronic; hepatitis c, chronic; liver cirrhosis; liver cirrhosis, alcoholic; liver failure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b, chronic; hepatitis c, chronic; liver cirrhosis; liver cirrhosis, alcoholic; liver failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b, chronic; hepatitis c, chronic; hepatitis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; liver carcinoma; liver cirrhosis; liver neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, hepatocellular; hepatitis b, chronic; hepatitis c, chronic; liver carcinoma; liver cirrhosis; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular remodeling Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; focal segmental glomsclerosis; glomerulosclerosis, focal segmental; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; chronic renal failure; hyperhomocysteinemia; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; chronic renal failure; hyperhomocysteinemia; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; glomerulonephritis, iga; iga glomerulonephritides; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; substance withdrawal syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; substance withdrawal syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia; chronic renal failure; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia; chronic renal failure; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hyperparathyroidism, secondary; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hyperparathyroidism, secondary; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic b-cell leukemias; leukemia, lymphocytic, chronic, b-cell; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic b-cell leukemias; leukemia, lymphocytic, chronic, b-cell; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension; kidney failure, chronic; lupus erythematosus, systemic; lupus nephritis; nephritis sle; systemic lupus erythematosus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; lupus erythematosus, systemic; lupus nephritis; nephritis sle; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertension, renal; kidney failure, chronic; renal hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic lymphocytic leukemia; leukemia, experimental; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic lymphocytic leukemia; leukemia, experimental; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; kidney failure, chronic; uremia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; kidney failure, chronic; uremia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hyperhomocysteinemia; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hyperhomocysteinemia; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; diabetic nephropathies; diabetic nephropathy; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; diabetic nephropathies; diabetic nephropathy; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic kidney insufficiency; diabetes mellitus type ii; diabetes mellitus, type 2; renal insufficiency, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hyperparathyroidism; kidney failure, chronic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hyperparathyroidism; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Chronic Prostatitis With Chronic Pelvic Pain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chronic Prostatitis With Chronic Pelvic Pain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chronic bronchitis and chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic bronchitis and chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic bronchitis in chronic obstructive pulmonary disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic bronchitis in chronic obstructive pulmonary disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
bone resorption; fractures, bone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone resorption; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone density; bone responsiveness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone density; bone responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal bone mineralization involved in bone maturation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bone mineralization involved in bone maturation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
negative regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of bone mineralization involved in bone maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of bone mineralization involved in bone maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Periodontitis, aggressive, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Periodontitis, aggressive, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Periodontitis, Aggressive, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Periodontitis, Aggressive, 2 from the curated CTD Gene-Disease Associations dataset. |
Periodontitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Periodontitis from the curated CTD Gene-Disease Associations dataset. |
Aggressive Periodontitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aggressive Periodontitis from the curated CTD Gene-Disease Associations dataset. |
Periapical Periodontitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Periapical Periodontitis from the curated CTD Gene-Disease Associations dataset. |
Periodontitis Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Periodontitis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
acute apical periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute apical periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
aggressive periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease aggressive periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
suppurative periapical periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease suppurative periapical periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
periapical periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease periapical periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lupus erythematosus; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lupus erythematosus; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; diabetes, type 2; blood pressure, arterial; liver disease; periodontitis; acenocoumarol response; acetaldehyde; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; diabetes, type 2; blood pressure, arterial; liver disease; periodontitis; acenocoumarol response; acetaldehyde; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periodontitis. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periodontitis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periodontitis, early-onset Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periodontitis, early-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periodontal diseases; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periodontal diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periodontitis; thromboangiitis obliterans Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periodontitis; thromboangiitis obliterans in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; periodontitis; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; periodontitis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aggressive periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fragile x syndrome; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fragile x syndrome; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periapical periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periapical periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; inflammation; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; inflammation; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lymphadenitis; mycobacterium infections; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lymphadenitis; mycobacterium infections; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gingival hemorrhage; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gingival hemorrhage; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dental plaque; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dental plaque; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dental plaque; periodontitis; pregnancy complications; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dental plaque; periodontitis; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; diabetes mellitus, type 2; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; diabetes mellitus, type 2; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early onset periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early onset periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
crohn disease; crohn's disease; periodontal pocket; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 2; periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
behcet syndrome; periodontitis; recurrence; stomatitis, aphthous Gene SetFrom GAD Gene-Disease Associations genes associated with the disease behcet syndrome; periodontitis; recurrence; stomatitis, aphthous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
early-onset periodontitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease early-onset periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
periodontitis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term periodontitis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Periodontitis (CDC/AAP) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Periodontitis (CDC/AAP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Periodontitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Periodontitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Periodontitis (Mean PAL) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Periodontitis (Mean PAL) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Periodontitis (PAL4Q3) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Periodontitis (PAL4Q3) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Periodontitis (DPAL) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Periodontitis (DPAL) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
periodontitis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease periodontitis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
periodontitis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the periodontitis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
periodontitis Gene SetFrom HPO Gene-Disease Associations genes associated with the periodontitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe periodontitis Gene SetFrom HPO Gene-Disease Associations genes associated with the severe periodontitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Periodontitis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Periodontitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Periodontitis, Juvenile Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Periodontitis, Juvenile phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aggressive Periodontitis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aggressive Periodontitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Periapical Periodontitis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Periapical Periodontitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
periodontitis 1, juvenile Gene SetFrom OMIM Gene-Disease Associations genes associated with the periodontitis 1, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset. |
periodontitis, aggressive, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the periodontitis, aggressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aggressive Periodontitis, Generalized Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aggressive Periodontitis, Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aggressive Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aggressive Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periapical Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periapical Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Suppurative Periapical Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Suppurative Periapical Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Rapidly Progressive Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Localized Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Localized Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Early Onset Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Early Onset Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Asymptomatic Periapical Periodontitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Asymptomatic Periapical Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodontitis, Acute Nonsuppurative Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodontitis, Acute Nonsuppurative in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodontitis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Periodontitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aggressive periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aggressive periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Periapical periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Periapical periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Suppurative periapical periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Suppurative periapical periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Acute apical periodontitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acute apical periodontitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Periodontitis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Periodontitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aggressive periodontitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aggressive periodontitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aggressive periodontitis (sex interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aggressive periodontitis (sex interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Periodontitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Periodontitis (DPAL) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontitis (DPAL) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Periodontitis (PAL4Q3) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontitis (PAL4Q3) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Periodontitis (Mean PAL) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontitis (Mean PAL) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Periodontitis (CDC/AAP) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontitis (CDC/AAP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Early onset periodontitis x smoking status interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early onset periodontitis x smoking status interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Periodontitis (stage III/IV grade C) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontitis (stage III/IV grade C) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
inactivation of gsk3 by akt causes accumulation of b-catenin in alveolar macrophages Gene SetFrom Biocarta Pathways proteins participating in the inactivation of gsk3 by akt causes accumulation of b-catenin in alveolar macrophages pathway from the Biocarta Pathways dataset. |
Pulmonary alveolar microlithiasis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary alveolar microlithiasis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alveolar capillary dysplasia with misalignment of pulmonary veins Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
alveolar lamellar body membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the alveolar lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
alveolar lamellar body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the alveolar lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
Pulmonary Alveolar Microlithiasis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Alveolar Microlithiasis from the curated CTD Gene-Disease Associations dataset. |
Rhabdomyosarcoma, Alveolar Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Rhabdomyosarcoma, Alveolar from the curated CTD Gene-Disease Associations dataset. |
Alveolar capillary dysplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alveolar capillary dysplasia from the curated CTD Gene-Disease Associations dataset. |
Sarcoma, Alveolar Soft Part Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sarcoma, Alveolar Soft Part from the curated CTD Gene-Disease Associations dataset. |
pulmonary alveolar proteinosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary alveolar proteinosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pulmonary alveolar microlithiasis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pulmonary alveolar microlithiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alveolar periostitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alveolar periostitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alveolar echinococcosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alveolar echinococcosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bronchiolo-alveolar adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bronchiolo-alveolar adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alveolar soft part sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alveolar soft part sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
alveolar rhabdomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alveolar rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
adenocarcinoma, bronchiolo-alveolar; hyperplasia; lung neoplasms; neoplasm of lung ; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma, bronchiolo-alveolar; hyperplasia; lung neoplasms; neoplasm of lung ; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenomatosis, pulmonary; lung neoplasms; neoplasm invasiveness; neoplasm of lung ; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenomatosis, pulmonary; lung neoplasms; neoplasm invasiveness; neoplasm of lung ; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar echinococcosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar echinococcosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma, bronchiolo-alveolar; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma, bronchiolo-alveolar; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alveolar Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term alveolar in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
c-Myc_OE_GDS3321_157_mouse_lung adenocarcinomas alveolar epithelia Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the c-Myc_OE_GDS3321_157_mouse_lung adenocarcinomas alveolar epithelia gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
STAT3_deficiency_GDS3106_58_mouse_type II alveolar cells Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the STAT3_deficiency_GDS3106_58_mouse_type II alveolar cells gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
alveolar secondary septum development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alveolar secondary septum development biological process from the curated GO Biological Process Annotations 2015 dataset. |
alveolar primary septum development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alveolar primary septum development biological process from the curated GO Biological Process Annotations 2015 dataset. |
alveolar lamellar body membrane Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the alveolar lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
alveolar lamellar body Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the alveolar lamellar body cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
abnormality of the alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
alveolar ridge overgrowth Gene SetFrom HPO Gene-Disease Associations genes associated with the alveolar ridge overgrowth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
alveolar soft part sarcoma Gene SetFrom HPO Gene-Disease Associations genes associated with the alveolar soft part sarcoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick anterior alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the thick anterior alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
alveolar cell carcinoma Gene SetFrom HPO Gene-Disease Associations genes associated with the alveolar cell carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
alveolar proteinosis Gene SetFrom HPO Gene-Disease Associations genes associated with the alveolar proteinosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cleft lower alveolar ridge Gene SetFrom HPO Gene-Disease Associations genes associated with the cleft lower alveolar ridge phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive alveolar ridge hypertropy Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive alveolar ridge hypertropy 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. |
broad alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the broad alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
alveolar rhabdomyosarcoma Gene SetFrom HPO Gene-Disease Associations genes associated with the alveolar rhabdomyosarcoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad secondary alveolar ridge Gene SetFrom HPO Gene-Disease Associations genes associated with the broad secondary alveolar ridge phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
alveolar ridge cleft Gene SetFrom HPO Gene-Disease Associations genes associated with the alveolar ridge cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Rhabdomyosarcoma, Alveolar Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Rhabdomyosarcoma, Alveolar phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Adenocarcinoma, Bronchiolo-Alveolar Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Adenocarcinoma, Bronchiolo-Alveolar phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pulmonary Alveolar Proteinosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pulmonary Alveolar Proteinosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
small alveolar lamellar bodies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal alveolar pore morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal alveolar pore morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal alveolar macrophage morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal alveolar macrophage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased alveolar lamellar body number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased alveolar lamellar body number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent alveolar lamellar bodies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
mammary gland alveolar hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the mammary gland alveolar hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal branching involved in alveolar sac morphogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal branching involved in alveolar sac morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar sac morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar sac morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal alveolar lamellar body morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal alveolar lamellar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary alveolar parenchyma morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary alveolar parenchyma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary alveolar proteinosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary alveolar proteinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal alveolar process morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal alveolar process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged alveolar lamellar bodies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary alveolar edema Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary alveolar edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated pulmonary alveolar ducts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated pulmonary alveolar ducts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased alveolar lamellar body number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased alveolar lamellar body number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent alveolar pores Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent alveolar pores phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary alveolar hemorrhage Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary alveolar hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
impaired branching involved in alveolar sac morphogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the impaired branching involved in alveolar sac morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent alveolar process Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent alveolar process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary alveolar microlithiasis Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary alveolar microlithiasis phenotype from the curated OMIM Gene-Disease Associations dataset. |
rhabdomyosarcoma 2, alveolar Gene SetFrom OMIM Gene-Disease Associations genes associated with the rhabdomyosarcoma 2, alveolar phenotype from the curated OMIM Gene-Disease Associations dataset. |
alveolar soft-part sarcoma Gene SetFrom OMIM Gene-Disease Associations genes associated with the alveolar soft-part sarcoma phenotype from the curated OMIM Gene-Disease Associations dataset. |
alveolar capillary dysplasia with misalignment of pulmonary veins Gene SetFrom OMIM Gene-Disease Associations genes associated with the alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated OMIM Gene-Disease Associations dataset. |
rhabdomyosarcoma, alveolar Gene SetFrom OMIM Gene-Disease Associations genes associated with the rhabdomyosarcoma, alveolar phenotype from the curated OMIM Gene-Disease Associations dataset. |
alveolar macrophage Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue alveolar macrophage from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
alveolar sac Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar sac in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar wall Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar wall in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar mucosa Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar epithelial cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar epithelial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar macrophage Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar macrophage in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar macrophage cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar macrophage cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar cell type ii Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar cell type ii in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
alveolar cell type i Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue alveolar cell type i in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Lung-alveolar fibroblast Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Lung-alveolar fibroblast relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Pulmonary Alveolar Proteinosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Alveolar Proteinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alveolar Capillary Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alveolar Capillary Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult Alveolar Soft Part Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult Alveolar Soft Part Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alveolar Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alveolar Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alveolar Soft Part Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alveolar Soft Part Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Alveolar Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Childhood Alveolar Soft Part Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Soft Part Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Alveolar Damage Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Alveolar Damage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Alveolar Hemorrhage Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Alveolar Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Alveolar Proteinosis, Congenital Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Alveolar Proteinosis, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Pulmonary Alveolar Proteinosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Pulmonary Alveolar Proteinosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alveolar Pyorrhea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alveolar Pyorrhea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Alveolar Hemorrhage Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Alveolar Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alveolar Ridge Abnormality Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alveolar Ridge Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pulmonary Alveolar Microlithiasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pulmonary Alveolar Microlithiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fusion-Negative Alveolar Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fusion-Negative Alveolar Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fusion-Positive Alveolar Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fusion-Positive Alveolar Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Alveolar Soft Part Sarcoma Metastatic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Alveolar Soft Part Sarcoma Metastatic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Unilateral Alveolar Cleft Of Maxilla Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Unilateral Alveolar Cleft Of Maxilla in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Alveolar Ridges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Alveolar Ridges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atrophy Of Alveolar Ridges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Alveolar Ridges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Anterior Alveolar Ridges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Anterior Alveolar Ridges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Midline Notch Of Upper Alveolar Ridge Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Midline Notch Of Upper Alveolar Ridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alveolar Ridge Overgrowth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alveolar Ridge Overgrowth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cleft Lower Alveolar Ridge Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Lower Alveolar Ridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Secondary Alveolar Ridge Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Secondary Alveolar Ridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Alveolar Ridge Hypertropy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Alveolar Ridge Hypertropy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cleft Alveolar Process Of Maxilla Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft Alveolar Process Of Maxilla in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
alveolar primary septum development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the alveolar primary septum development biological process from the curated GO Biological Process Annotations 2023 dataset. |
alveolar lamellar body Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the alveolar lamellar body cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
alveolar lamellar body membrane Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the alveolar lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
abnormal pulmonary alveolar sac morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pulmonary alveolar sac morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired branching involved in alveolar sac morphogenesis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired branching involved in alveolar sac morphogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pulmonary alveolar hemorrhage Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary alveolar hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
alveolar process atrophy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the alveolar process atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent alveolar process Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent alveolar process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pulmonary alveolar parenchyma morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pulmonary alveolar parenchyma morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased alveolar lamellar body number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased alveolar lamellar body number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged alveolar lamellar bodies Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased alveolar lamellar body number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased alveolar lamellar body number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated pulmonary alveolar duct Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated pulmonary alveolar duct phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal alveolar process morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal alveolar process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal alveolar macrophage morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal alveolar macrophage morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal alveolar lamellar body morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal alveolar lamellar body morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pulmonary alveolar proteinosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary alveolar proteinosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
mammary gland alveolar hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the mammary gland alveolar hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small alveolar lamellar bodies Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal branching involved in alveolar duct morphogenesis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal branching involved in alveolar duct morphogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pulmonary alveolar duct morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pulmonary alveolar duct morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pulmonary alveolar edema Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pulmonary alveolar edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent alveolar lamellar bodies Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent alveolar lamellar bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent alveolar pores Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent alveolar pores phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pulmonary alveolar system morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pulmonary alveolar system morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal alveolar pore morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal alveolar pore morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased alveolar macrophage number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased alveolar macrophage number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased alveolar macrophage number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased alveolar macrophage number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Fetal Development - L1 - Bronchiolar and alveolar epithelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Bronchiolar and alveolar epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Lung-Bronchiolar and alveolar epithelial cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Bronchiolar and alveolar epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v1 - L1 - Alveolar Epithelial Type 1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L1 - Alveolar Epithelial Type 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v1 - L1 - Alveolar Epithelial Type 2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L1 - Alveolar Epithelial Type 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v1 - L2 - Alveolar Epithelial Type 1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Alveolar Epithelial Type 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v1 - L2 - Alveolar Fibroblast Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Alveolar Fibroblast cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v1 - L2 - Alveolar Epithelial Type 2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Alveolar Epithelial Type 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v1 - L2 - Signaling Alveolar Epithelial Type 2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Signaling Alveolar Epithelial Type 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - L2 - Alveolar epithelium Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L2 - Alveolar epithelium cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - L4 - Alveolar macrophages Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L4 - Alveolar macrophages cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - L4 - Alveolar fibroblasts Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L4 - Alveolar fibroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - L5 - Alveolar Mφ CCL3+ Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L5 - Alveolar Mφ CCL3+ cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - L5 - Alveolar Mφ proliferating Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L5 - Alveolar Mφ proliferating cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - L5 - Alveolar Mφ MT-positive Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - L5 - Alveolar Mφ MT-positive cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - Finest - Alveolar macrophages Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - Finest - Alveolar macrophages cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - Finest - Alveolar Mφ CCL3+ Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - Finest - Alveolar Mφ CCL3+ cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - Finest - Alveolar Mφ proliferating Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - Finest - Alveolar Mφ proliferating cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - Finest - Alveolar fibroblasts Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - Finest - Alveolar fibroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v2 (HLCA) - Finest - Alveolar Mφ MT-positive Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v2 (HLCA) - Finest - Alveolar Mφ MT-positive cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Alveolar type II (ATII) cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar type II (ATII) cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar cell Type 1_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar cell Type 1_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Macrophage_Mandibular alveolar bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Macrophage_Mandibular alveolar bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Natural killer cell_Mandibular alveolar bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Natural killer cell_Mandibular alveolar bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
T cell_Mandibular alveolar bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the T cell_Mandibular alveolar bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Megakaryocyte_Mandibular alveolar bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Megakaryocyte_Mandibular alveolar bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Mesenchymal cell_Mandibular alveolar bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Mesenchymal cell_Mandibular alveolar bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Neutrophil_Mandibular alveolar bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Neutrophil_Mandibular alveolar bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Myeloid cell_Mandibular alveolar bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Myeloid cell_Mandibular alveolar bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar macrophage_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar macrophage_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar epithelial progenitor cell_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar epithelial progenitor cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar pneumocyte Type II_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar pneumocyte Type II_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar type II (ATII) cell_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar type II (ATII) cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar macrophage_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar macrophage_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar cell Type 1_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar cell Type 1_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar pneumocyte Type I_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar pneumocyte Type I_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar cell_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar cell Type 2_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar cell Type 2_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar epithelial cell Type 1_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar epithelial cell Type 1_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar epithelial cell Type 2_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar epithelial cell Type 2_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar pneumocyte Type II_Alveolus_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar pneumocyte Type II_Alveolus_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar pneumocyte Type I_Alveolus_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar pneumocyte Type I_Alveolus_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Early type I alveolar pneumocyte_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Early type I alveolar pneumocyte_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Late type I alveolar pneumocyte_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Late type I alveolar pneumocyte_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Mature type I alveolar pneumocyte_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Mature type I alveolar pneumocyte_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Naive type II alveolar pneumocyte_Alveolus_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Naive type II alveolar pneumocyte_Alveolus_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Pulmonary alveolar cell Type 2_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pulmonary alveolar cell Type 2_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar macrophage_Bronchoalveolar system_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar macrophage_Bronchoalveolar system_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar capillary cell_Alveolar capillary_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar capillary cell_Alveolar capillary_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar epithelial cell Type 2_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar epithelial cell Type 2_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar epithelial cell Type 1_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar epithelial cell Type 1_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar type II (ATII) cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar type II (ATII) cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Differentiated alveolar epithelial cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Differentiated alveolar epithelial cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar type 2-like cell_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar type 2-like cell_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar pneumocyte Type I_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar pneumocyte Type I_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar pneumocyte Type II_Lung_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar pneumocyte Type II_Lung_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar cell Type 1_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar cell Type 1_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar progenitor cell_Mammary gland_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar progenitor cell_Mammary gland_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Differentiated alveolar cell_Mammary gland_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Differentiated alveolar cell_Mammary gland_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar macrophage_Sputum_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar macrophage_Sputum_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Alveolar epithelial cell Type 2_Undefined_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Alveolar epithelial cell Type 2_Undefined_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM) Gene Setproteins participating in the Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM) pathway from the Reactome Pathways 2024 dataset. |
alveolar primary septum development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the alveolar primary septum development biological process from the curated GO Biological Process Annotations 2025 dataset. |
alveolar lamellar body Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the alveolar lamellar body cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
alveolar lamellar body membrane Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the alveolar lamellar body membrane cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Pulmonary alveolar microlithiasis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pulmonary alveolar microlithiasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Pulmonary alveolar proteinosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary alveolar proteinosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pulmonary alveolar microlithiasis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulmonary alveolar microlithiasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alveolar echinococcosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alveolar echinococcosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alveolar soft part sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alveolar soft part sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alveolar rhabdomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alveolar rhabdomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
bronchiolo-alveolar adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease bronchiolo-alveolar adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alveolar periostitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alveolar periostitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Alveolar macrophage Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Alveolar macrophage from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar sac Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar sac in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar wall Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar wall in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar macrophage Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar macrophage in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar cell type II Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar cell type II in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar epithelial cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar epithelial cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar macrophage cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar macrophage cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar mucosa Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar mucosa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar cell type I Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Alveolar cell type I in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Alveolar lamellar body membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Alveolar lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Alveolar lamellar body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Alveolar lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Alveolar lamellar body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Alveolar lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Alveolar lamellar body membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Alveolar lamellar body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Hereditary pulmonary alveolar proteinosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary pulmonary alveolar proteinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alveolar capillary dysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alveolar capillary dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Alveolar rhabdomyosarcoma Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Alveolar rhabdomyosarcoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PULMONARY ALVEOLAR MICROLITHIA Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the PULMONARY ALVEOLAR MICROLITHIA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations 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. |
Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss 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. |
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
DFNA 2 Nonsyndromic Hearing Loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the DFNA 2 Nonsyndromic Hearing Loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Split-hand/foot malformation 1 with sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Camptodactyly, tall stature, and hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hearing Loss, Sudden Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hearing Loss, Sudden from the curated CTD Gene-Disease Associations dataset. |
Blood Loss, Surgical Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Blood Loss, Surgical from the curated CTD Gene-Disease Associations dataset. |
Hearing Loss Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hearing Loss from the curated CTD Gene-Disease Associations dataset. |
HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset. |
Tooth Loss Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tooth Loss from the curated CTD Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset. |
Progressive hearing loss stapes fixation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Progressive hearing loss stapes fixation from the curated CTD Gene-Disease Associations dataset. |
Hearing Loss, Conductive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hearing Loss, Conductive from the curated CTD Gene-Disease Associations dataset. |
Hearing Loss, Sensorineural Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hearing Loss, Sensorineural from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset. |
Weight Loss Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Weight Loss from the curated CTD Gene-Disease Associations dataset. |
Hearing Loss, Bilateral Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hearing Loss, Bilateral from the curated CTD Gene-Disease Associations dataset. |
Hearing Loss, Noise-Induced Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hearing Loss, Noise-Induced from the curated CTD Gene-Disease Associations dataset. |
Embryo Loss Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Embryo Loss from the curated CTD Gene-Disease Associations dataset. |
Hearing Loss Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Hearing Loss in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
sensorineural hearing loss Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sensorineural hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; overweight; weight gain; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; overweight; weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss/deafness; osteogenesis imperfecta Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss/deafness; osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
inflammation; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease inflammation; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; otosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; otosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complete hearing loss; deafness; vestibular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; vestibular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, second trimester Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, second trimester in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, central Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autosomal dominant hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autosomal dominant hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; overweight; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; overweight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
mouth, edentulous; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease mouth, edentulous; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; obesity, morbid; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
embryo loss; fetal death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease embryo loss; fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; weight gain; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
h-ras allele loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease h-ras allele loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; coagulation disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; rhinitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural nonsyndromic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural nonsyndromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
goiter; hearing loss, sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease goiter; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood loss, surgical Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood loss, surgical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal loss, late Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal loss, late in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dominant non-syndromic sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dominant non-syndromic sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing disorders; hearing loss, high-frequency; hearing problem Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing disorders; hearing loss, high-frequency; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss/deafness; retinal disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss/deafness; retinal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
goiter; hearing loss, sensorineural; vertigo Gene SetFrom GAD Gene-Disease Associations genes associated with the disease goiter; hearing loss, sensorineural; vertigo in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
deafness; hearing loss, sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease deafness; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, unilateral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, unilateral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
unresolved loss or trauma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease unresolved loss or trauma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome; pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dna damage; embryo loss; hyperhomocysteinemia; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dna damage; embryo loss; hyperhomocysteinemia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sudden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; in vitro fertilization success Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; in vitro fertilization success in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal loss, early Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal loss, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity, morbid; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; infant, premature, diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; infant, premature, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genetic diseases, inborn; hearing impairment; hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genetic diseases, inborn; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent early fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent early fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss/deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss/deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nonsyndromic hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nonsyndromic hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
weight gain; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal loss ; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal loss ; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, nonsyndromic sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, nonsyndromic sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin resistance; overweight; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin resistance; overweight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced intrapartum blood loss--a possible evolutionary selection mechanism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced intrapartum blood loss--a possible evolutionary selection mechanism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, bilateral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, bilateral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; insulin resistance; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; embryo loss; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; embryo loss; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
embryo loss; habitual aborter nos; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease embryo loss; habitual aborter nos; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
deafness; hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease deafness; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; fatty liver; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; fatty liver; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
goiter; hearing loss, sensorineural; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease goiter; hearing loss, sensorineural; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; weight loss; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; weight loss; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, noise-induced; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, noise-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, noise-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sudden; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lumen loss, late Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lumen loss, late in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity, abdominal; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity, abdominal; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antisense paternal transcript and loss of imprinting Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antisense paternal transcript and loss of imprinting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity, morbid; postoperative complications; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity, morbid; postoperative complications; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
unexplained foetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease unexplained foetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss; noonan syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss; noonan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
presbycusis; hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease presbycusis; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent pregnancy loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent pregnancy loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
loss Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term loss in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of water loss via skin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of water loss via skin biological process from the curated GO Biological Process Annotations 2015 dataset. |
Weight loss (gastric bypass surgery) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Weight loss (gastric bypass surgery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
weight loss Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the weight loss phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
loss of ability to walk Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of ability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of ability to walk in first decade Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of ability to walk in first decade phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-frequency hearing loss Gene SetFrom HPO Gene-Disease Associations genes associated with the low-frequency hearing loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of facial expression Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature loss of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the premature loss of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of voice Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of voice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of subcutaneous adipose tissue in limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of subcutaneous adipose tissue in limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent loss of toenails and fingernails Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent loss of toenails and fingernails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weight loss Gene SetFrom HPO Gene-Disease Associations genes associated with the weight loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of truncal subcutaneous adipose tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of truncal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
axonal loss Gene SetFrom HPO Gene-Disease Associations genes associated with the axonal loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scalp hair loss Gene SetFrom HPO Gene-Disease Associations genes associated with the scalp hair loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sudden central visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the sudden central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive central visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cranial nerve motor loss Gene SetFrom HPO Gene-Disease Associations genes associated with the cranial nerve motor loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of speech Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of speech phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nonprogressive visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the nonprogressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neuronal loss in the cerebral cortex Gene SetFrom HPO Gene-Disease Associations genes associated with the neuronal loss in the cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neuronal loss in basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the neuronal loss in basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature loss of permanent teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the premature loss of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature loss of primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the premature loss of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal cord posterior columns myelin loss Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal cord posterior columns myelin loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of ability to walk in early childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of consciousness Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of consciousness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neuronal loss in central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the neuronal loss in central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of facial adipose tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of facial adipose tissue 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. |
loss of gluteal subcutaneous adipose tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of gluteal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory loss of all modalities Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of purkinje cells in the cerebellar vermis Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of purkinje cells in the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adipose tissue loss Gene SetFrom HPO Gene-Disease Associations genes associated with the adipose tissue loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Blood Loss, Surgical Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Blood Loss, Surgical phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Central Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Tooth Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Unilateral Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Unilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Functional Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Functional phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Sensorineural Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Weight Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Weight Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Mixed Conductive-Sensorineural Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Mixed Conductive-Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Bilateral Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Bilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Noise-Induced Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Noise-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, High-Frequency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, High-Frequency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Periodontal Attachment Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Periodontal Attachment Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Sudden Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Embryo Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Embryo Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
syndromic hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the syndromic hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
conductive hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the conductive hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
loss of gabaergic neurons Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the loss of gabaergic neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased susceptibility to ototoxicity-induced hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to ototoxicity-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
sensorineural hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sensorineural hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased susceptibility to weight loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
loss of vibrissae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the loss of vibrissae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
loss of glutamate neurons Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the loss of glutamate neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
loss of dopaminergic neurons Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the loss of dopaminergic neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
loss of hippocampal neurons Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the loss of hippocampal neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
proximal convoluted tubule brush border loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
weight loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased susceptibility to weight loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
partial loss of secondary muscle spindle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
loss of basal ganglia neurons Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the loss of basal ganglia neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
nonsyndromic hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the nonsyndromic hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased susceptibility to age-related hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to age-related hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
premature hair loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the premature hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
loss of eyelid cilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the loss of eyelid cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
focal dorsal hair loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased susceptibility to noise-induced hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
focal hair loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the focal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
progressive hair loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the progressive hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased susceptibility to noise-induced hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
loss of cortex neurons Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the loss of cortex neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal susceptibility to weight loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal susceptibility to hearing loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal susceptibility to hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
{pregnancy loss, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset. |
?split-hand/foot malformation 1 with sensorineural hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{bulimia nervosa, age of onset of weight loss in} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {bulimia nervosa, age of onset of weight loss in} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{?hearing loss, cisplatin-induced, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {?hearing loss, cisplatin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene SetFrom OMIM Gene-Disease Associations genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset. |
ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
congenital cataracts, hearing loss, and neurodegeneration Gene SetFrom OMIM Gene-Disease Associations genes associated with the congenital cataracts, hearing loss, and neurodegeneration phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 2} 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. |
Loss of Function of SMAD4 in Cancer Gene Setproteins participating in the Loss of Function of SMAD4 in Cancer pathway from the Reactome Pathways dataset. |
Loss of Function of TGFBR2 in Cancer Gene Setproteins participating in the Loss of Function of TGFBR2 in Cancer pathway from the Reactome Pathways dataset. |
Loss of Nlp from mitotic centrosomes Gene Setproteins participating in the Loss of Nlp from mitotic centrosomes pathway from the Reactome Pathways dataset. |
Loss of Function of TGFBR1 in Cancer Gene Setproteins participating in the Loss of Function of TGFBR1 in Cancer pathway from the Reactome Pathways dataset. |
Loss of proteins required for interphase microtubule organization from the centrosome Gene Setproteins participating in the Loss of proteins required for interphase microtubule organization from the centrosome pathway from the Reactome Pathways dataset. |
Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling Gene Setproteins participating in the Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling pathway from the Reactome Pathways dataset. |
Loss of Function of SMAD2/3 in Cancer Gene Setproteins participating in the Loss of Function of SMAD2/3 in Cancer pathway from the Reactome Pathways dataset. |
Sensorineural Hearing Loss (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Hearing Loss (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Conductive Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Conductive Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sensorineural Hearing Loss, Bilateral Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Hearing Loss, Bilateral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sensory Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sensory Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dominant Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dominant Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hearing Loss, Cisplatin-Induced, Susceptibility To Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hearing Loss, Cisplatin-Induced, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loss Of Hypoglycemic Warning Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Loss Of Hypoglycemic Warning in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tooth Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tooth Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sudden Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sudden Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Profound Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Profound Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Conductive Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Conductive Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Noise-Induced Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Noise-Induced Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Split-Hand-Foot Malformation With Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Split-Hand-Foot Malformation With Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Inherited Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Inherited Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autoimmune Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodontal Attachment Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Attachment Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pregnancy Loss, Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pregnancy Loss, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bilateral Sensory Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Sensory Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Hearing Loss Stapes Fixation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Hearing Loss Stapes Fixation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recessive Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recessive Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Nonscarring Hair Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Nonscarring Hair Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Volume Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Volume Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Epithelial Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Epithelial Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loss Of Skin Elasticity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Loss Of Skin Elasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loss Of Cervical Lordosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Loss Of Cervical Lordosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paragangliomas With Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paragangliomas With Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Cataracts, Hearing Loss, And Neurodegeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cataracts, Hearing Loss, And Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loss Of Speech Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Speech in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unspecified Visual Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unspecified Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Early Pregnancy Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Pregnancy Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Memory Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Memory Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Ability To Walk Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Visual Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neuronal Loss In Central Nervous System Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Axonal Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Loss 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. |
Loss Of Subcutaneous Adipose Tissue In Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Subcutaneous Adipose Tissue In Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sudden Loss Of Visual Acuity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Loss Of Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Complete Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Premature Loss Of Permanent Teeth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Loss Of Permanent Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pregnancy Loss, Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pregnancy Loss, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Memory Ability Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Memory Ability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Purkinje Cells In The Cerebellar Vermis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Purkinje Cells In The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spinal Cord Posterior Columns Myelin Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Cord Posterior Columns Myelin Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Premature Tooth Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Tooth Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neuronal Loss In The Cerebral Cortex Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In The Cerebral Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sensorineural Hearing Loss, Progressive Bilateral Postlingual Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sensorineural Hearing Loss, Progressive Bilateral Postlingual in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Severe Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Gluteal Subcutaneous Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Gluteal Subcutaneous Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Scalp Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Scalp Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Ability To Walk In Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk In Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Facial Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Facial Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Acquired Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acquired Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Embryo Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Embryo Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Foveal Photoreceptor Outer Segment Loss On Macular Oct Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foveal Photoreceptor Outer Segment Loss On Macular Oct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Photoreceptor Layer Loss On Macular Oct Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Photoreceptor Layer Loss On Macular Oct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nail Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nail Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Facial Expression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Facial Expression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neuronal Loss In Basal Ganglia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Adipose Tissue Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adipose Tissue Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Loss Of Toenails And Fingernails Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Loss Of Toenails And Fingernails in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Truncal Subcutaneous Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Truncal Subcutaneous Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Subcutaneous Adipose Tissue From Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Subcutaneous Adipose Tissue From Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Loss Of Facial Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Loss Of Facial Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Ability To Walk In First Decade Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk In First Decade in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nonprogressive Visual Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonprogressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sudden Visual Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Proprioception Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Proprioception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pre-Ictal Memory Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pre-Ictal Memory Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Retrograde Memory Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retrograde Memory Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nonsyndromic Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonsyndromic Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cranial Nerve Motor Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cranial Nerve Motor Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
weight loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the weight loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of eyelid cilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of eyelid cilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
premature hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the premature hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to noise-induced hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of dopaminergic neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of dopaminergic neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
sensorineural hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the sensorineural hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
proximal convoluted tubule brush border loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
partial loss of secondary muscle spindle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of hippocampal neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of hippocampal neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to weight loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to weight loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to age-related hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to age-related hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
nonsyndromic hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the nonsyndromic hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
progressive hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
conductive hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the conductive hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in head/neck region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in head/neck region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal dorsal hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of glutamate neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of glutamate neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to ototoxicity-induced hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to ototoxicity-induced hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
syndromic hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the syndromic hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to noise-induced hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of basal ganglia neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of basal ganglia neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of cortex neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of cortex neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of GABAergic neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of GABAergic neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal susceptibility to hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal susceptibility to hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of vibrissae Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of vibrissae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to weight loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to weight loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed suckling reflex loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed suckling reflex loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
mixed hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the mixed hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in abdominal region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in abdominal region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
premature suckling reflex loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the premature suckling reflex loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in thorax region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in thorax region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Defective DNA double strand break response due to BARD1 loss of function Gene Setproteins participating in the Defective DNA double strand break response due to BARD1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective DNA double strand break response due to BRCA1 loss of function Gene Setproteins participating in the Defective DNA double strand break response due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function Gene Setproteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function pathway from the Reactome Pathways 2024 dataset. |
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function Gene Setproteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function pathway from the Reactome Pathways 2024 dataset. |
Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function Gene Setproteins participating in the Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to BRCA1 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to BRCA2 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to BRCA2 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to PALB2 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to PALB2 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to ABCA4 loss of function Gene Setproteins participating in the Defective visual phototransduction due to ABCA4 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to LRAT loss of function Gene Setproteins participating in the Defective visual phototransduction due to LRAT loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1LW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1LW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1MW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1MW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1SW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1SW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to RDH12 loss of function Gene Setproteins participating in the Defective visual phototransduction due to RDH12 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to RDH5 loss of function Gene Setproteins participating in the Defective visual phototransduction due to RDH5 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to STRA6 loss of function Gene Setproteins participating in the Defective visual phototransduction due to STRA6 loss of function pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling Gene Setproteins participating in the Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of SMAD2/3 in Cancer Gene Setproteins participating in the Loss of Function of SMAD2/3 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of SMAD4 in Cancer Gene Setproteins participating in the Loss of Function of SMAD4 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of TGFBR1 in Cancer Gene Setproteins participating in the Loss of Function of TGFBR1 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of TGFBR2 in Cancer Gene Setproteins participating in the Loss of Function of TGFBR2 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of TP53 in Cancer Gene Setproteins participating in the Loss of Function of TP53 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of MECP2 binding ability to 5hmC-DNA Gene Setproteins participating in the Loss of MECP2 binding ability to 5hmC-DNA pathway from the Reactome Pathways 2024 dataset. |
Loss of MECP2 binding ability to 5mC-DNA Gene Setproteins participating in the Loss of MECP2 binding ability to 5mC-DNA pathway from the Reactome Pathways 2024 dataset. |
Loss of MECP2 binding ability to the NCoR/SMRT complex Gene Setproteins participating in the Loss of MECP2 binding ability to the NCoR/SMRT complex pathway from the Reactome Pathways 2024 dataset. |
Loss of Nlp from mitotic centrosomes Gene Setproteins participating in the Loss of Nlp from mitotic centrosomes pathway from the Reactome Pathways 2024 dataset. |
Loss of function of MECP2 in Rett syndrome Gene Setproteins participating in the Loss of function of MECP2 in Rett syndrome pathway from the Reactome Pathways 2024 dataset. |
Loss of phosphorylation of MECP2 at T308 Gene Setproteins participating in the Loss of phosphorylation of MECP2 at T308 pathway from the Reactome Pathways 2024 dataset. |
Loss of proteins required for interphase microtubule organization from the centrosome Gene Setproteins participating in the Loss of proteins required for interphase microtubule organization from the centrosome pathway from the Reactome Pathways 2024 dataset. |
Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD Gene Setproteins participating in the Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD pathway from the Reactome Pathways 2024 dataset. |
Loss-of-function mutations in DBT cause MSUD2 Gene Setproteins participating in the Loss-of-function mutations in DBT cause MSUD2 pathway from the Reactome Pathways 2024 dataset. |
Loss-of-function mutations in DLD cause MSUD3/DLDD Gene Setproteins participating in the Loss-of-function mutations in DLD cause MSUD3/DLDD pathway from the Reactome Pathways 2024 dataset. |
PTEN Loss of Function in Cancer Gene Setproteins participating in the PTEN Loss of Function in Cancer pathway from the Reactome Pathways 2024 dataset. |
RAS signaling downstream of NF1 loss-of-function variants Gene Setproteins participating in the RAS signaling downstream of NF1 loss-of-function variants pathway from the Reactome Pathways 2024 dataset. |
Sensorineural hearing loss Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sensorineural hearing loss in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sensorineural hearing loss Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensorineural hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
drug-induced hearing loss Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease drug-induced hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation 1 with sensorineural hearing loss Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 1 with sensorineural hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
camptodactyly-tall stature-scoliosis-hearing loss syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease camptodactyly-tall stature-scoliosis-hearing loss syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Short stature, hearing loss, retinitis pigmentosa, and distinctive facies Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short stature, hearing loss, retinitis pigmentosa, and distinctive facies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive nonsyndromic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive nonsyndromic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pregnancy loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pregnancy loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sensorineural hearing loss disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensorineural hearing loss disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant nonsyndromic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant nonsyndromic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nonsyndromic genetic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonsyndromic genetic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood onset hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked mixed hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked mixed hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary hearing loss and deafness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary hearing loss and deafness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome 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. |
Camptodactyly-tall stature-scoliosis-hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Camptodactyly-tall stature-scoliosis-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant keratitis-ichthyosis-hearing loss syndrome 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. |
Nonsyndromic Hearing Loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonsyndromic Hearing Loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nonsyndromic sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonsyndromic sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Visual loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Noise induced hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Noise induced hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Loss of ambulation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Loss of ambulation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hearing loss and Retinal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hearing loss and Retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked nonsyndromic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked nonsyndromic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cone-rod dystrophy and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cone-rod dystrophy and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hearing loss in noise exposure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hearing loss in noise exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Trans-epidermal water loss Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Trans-epidermal water loss phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mosaic loss of chromosome Y (Y chromosome dosage) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mosaic loss of chromosome Y (Y chromosome dosage) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Weight loss (gastric bypass surgery) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Weight loss (gastric bypass surgery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mosaic loss of chromosome Y Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mosaic loss of chromosome Y phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hearing loss in Charcot-Marie-Tooth disease 1A Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hearing loss in Charcot-Marie-Tooth disease 1A phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cisplatin-induced hearing loss in childhood cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cisplatin-induced hearing loss in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neutropenia, nonimmune chronic idiopathic, of adults Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neutropenia, nonimmune chronic idiopathic, of adults phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intestinal pseudoobstruction neuronal chronic idiopathic X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intestinal pseudoobstruction neuronal chronic idiopathic X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Idiopathic fibrosing alveolitis, chronic form Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Idiopathic fibrosing alveolitis, chronic form phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gm2-gangliosidosis, chronic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gm2-gangliosidosis, chronic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sandhoff disease, chronic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sandhoff disease, chronic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Chronic Pain Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Chronic Pain from the curated CTD Gene-Disease Associations dataset. |
Bronchitis, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bronchitis, Chronic from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I from the curated CTD Gene-Disease Associations dataset. |
Drug-Induced Liver Injury, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Drug-Induced Liver Injury, Chronic from the curated CTD Gene-Disease Associations dataset. |
Pulmonary Disease, Chronic Obstructive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pulmonary Disease, Chronic Obstructive from the curated CTD Gene-Disease Associations dataset. |
Candidiasis familial chronic mucocutaneous, autosomal recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, autosomal recessive from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative from the curated CTD Gene-Disease Associations dataset. |
Hepatitis B, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatitis B, Chronic from the curated CTD Gene-Disease Associations dataset. |
Kidney Failure, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Kidney Failure, Chronic from the curated CTD Gene-Disease Associations dataset. |
Pancreatitis, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pancreatitis, Chronic from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II from the curated CTD Gene-Disease Associations dataset. |
Brain Damage, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Damage, Chronic from the curated CTD Gene-Disease Associations dataset. |
Hepatitis C, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatitis C, Chronic from the curated CTD Gene-Disease Associations dataset. |
Myeloproliferative Disorder, Chronic, with Eosinophilia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myeloproliferative Disorder, Chronic, with Eosinophilia from the curated CTD Gene-Disease Associations dataset. |
Leukemia, Myelomonocytic, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukemia, Myelomonocytic, Chronic from the curated CTD Gene-Disease Associations dataset. |
Candidiasis, Chronic Mucocutaneous Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Candidiasis, Chronic Mucocutaneous from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic from the curated CTD Gene-Disease Associations dataset. |
Leukemia, Lymphocytic, Chronic, B-Cell Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukemia, Lymphocytic, Chronic, B-Cell from the curated CTD Gene-Disease Associations dataset. |
Neutropenia, Nonimmune Chronic Idiopathic, Adult Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutropenia, Nonimmune Chronic Idiopathic, Adult from the curated CTD Gene-Disease Associations dataset. |
Renal Insufficiency, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Insufficiency, Chronic from the curated CTD Gene-Disease Associations dataset. |
Hepatitis, Chronic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hepatitis, Chronic from the curated CTD Gene-Disease Associations dataset. |
PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset. |
Leukemia, Myelogenous, Chronic, BCR-ABL Positive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukemia, Myelogenous, Chronic, BCR-ABL Positive from the curated CTD Gene-Disease Associations dataset. |
Jaundice, Chronic Idiopathic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Jaundice, Chronic Idiopathic from the curated CTD Gene-Disease Associations dataset. |
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative from the curated CTD Gene-Disease Associations dataset. |
Ophthalmoplegia, Chronic Progressive External Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, Chronic Progressive External from the curated CTD Gene-Disease Associations dataset. |
Granulomatous Disease, Chronic, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granulomatous Disease, Chronic, X-Linked from the curated CTD Gene-Disease Associations dataset. |
Hepatitis B, Chronic Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Hepatitis B, Chronic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Hepatitis C, Chronic Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Hepatitis C, Chronic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Kidney Failure, Chronic Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Kidney Failure, Chronic in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Leukemia, Myeloid, Chronic-Phase Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Leukemia, Myeloid, Chronic-Phase in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Pulmonary Disease, Chronic Obstructive Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Pulmonary Disease, Chronic Obstructive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Leukemia, Lymphocytic, Chronic, B-Cell Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Leukemia, Lymphocytic, Chronic, B-Cell in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
chronic progressive external ophthalmoplegia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
chronic myeloproliferative disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic myeloproliferative disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
chronic granulomatous disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic granulomatous disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
chronic pulmonary heart disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic pulmonary heart disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
chronic kidney failure Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease chronic kidney failure in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
chronic obstructive pulmonary disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease chronic obstructive pulmonary disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
chronic gonococcal salpingitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic gonococcal salpingitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic eosinophilic pneumonia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic eosinophilic pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic purulent otitis media Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic purulent otitis media in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic monocytic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic monocytic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic wasting disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic wasting disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
chronic leukemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |