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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. |
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. |
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. |
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. |
hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pregnancy complications, hematologic; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pregnancy complications, hematologic; thromboembolism 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. |
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. |
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. |
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. |
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. |
{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. |
{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. |
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. |
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. |
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. |
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. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; puerperal disorders; pulmonary embolism; pulmonary embolisms; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; pulmonary embolism; pulmonary embolisms; recurrence; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension induced by pregnancy; hypertension, pregnancy-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arteriosclerosis; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arteriosclerosis; complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; pregnancy complications, cardiovascular; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus, type 1; gastroenteritis; pregnancy complications, infectious; pregnancy in diabetics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 1; gastroenteritis; pregnancy complications, infectious; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hyperglycemia; pregnancy complications; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; hypertension; pregnancy complications, cardiovascular 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. |
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. |
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. |
{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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
Cholestasis, intrahepatic, of pregnancy 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cholestasis, intrahepatic, of pregnancy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cholestasis of pregnancy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cholestasis of pregnancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrahepatic Cholestasis of Pregnancy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Intrahepatic Cholestasis of Pregnancy from the curated CTD Gene-Disease Associations dataset. |
Pregnancy Complications Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pregnancy Complications from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset. |
Hypertension, Pregnancy-Induced Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertension, Pregnancy-Induced from the curated CTD Gene-Disease Associations dataset. |
Pregnancy, Ectopic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pregnancy, Ectopic from the curated CTD Gene-Disease Associations dataset. |
Pregnancy Complications, Cardiovascular Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pregnancy Complications, Cardiovascular from the curated CTD Gene-Disease Associations dataset. |
pregnancy adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pregnancy adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hemochromatosis; precursor cell lymphoblastic leukemia-lymphoma; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pre-eclampsia; pregnancy complications; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pre-eclampsia; pregnancy complications; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; puerperal disorders; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; puerperal disorders; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
rhd-negative sensitized pregnancy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease rhd-negative sensitized pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hiv infections; pregnancy complications, infectious; viremia; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv infections; pregnancy complications, infectious; viremia; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; activated protein c resistance; placenta abruptio; pregnancy complications, hematologic; recurrence; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; activated protein c resistance; placenta abruptio; pregnancy complications, hematologic; recurrence; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hiv infections; pregnancy complications, infectious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv infections; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
preeclampsia; hypertension, pregnancy induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease preeclampsia; hypertension, pregnancy induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pre-eclampsia; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, infectious; vaginosis, bacterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, infectious; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hemorrhage; pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malaria, falciparum; pregnancy complications, parasitic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications; prenatal exposure delayed effects; serotonin syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications; prenatal exposure delayed effects; serotonin syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholestasis, intrahepatic; pregnancy complications; pruritus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; pregnancy complications; pruritus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nausea; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nausea; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; pregnancy complications; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; pregnancy complications; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; pregnancy complications, cardiovascular; premature birth; stroke Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; pregnancy complications, cardiovascular; premature birth; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eclampsia; hypertension, pregnancy-induced; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eclampsia; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis, rheumatoid; pregnancy complications; puerperal disorders; recurrence; rheumatoid arthritis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; pregnancy complications; puerperal disorders; recurrence; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia in pregnancy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia in pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis b; pregnancy complications, infectious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis b; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertriglyceridemia; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertriglyceridemia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications; tic disorder; tic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications; tic disorder; tic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy-induced chylomicronemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy-induced chylomicronemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hellp syndrome; acute fatty liver of pregnancy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hellp syndrome; acute fatty liver of pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal death; pre-eclampsia; pregnancy complications; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholestasis, intrahepatic; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy-induced; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholestasis, intrahepatic; infant, premature, diseases; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; infant, premature, diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; hyperglycemia; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; hyperglycemia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy-induced; pre-eclampsia; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy outcome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy outcome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; hypertriglyceridemia; pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malaria, falciparum; placenta diseases; pregnancy complications, parasitic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; placenta diseases; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pre-eclampsia; pregnancy complications, cardiovascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pre-eclampsia; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; pregnancy complications, hematologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; pregnancy complications, cardiovascular Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; pregnancy complications, cardiovascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; pregnancy complications; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; pregnancy complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; overnutrition; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; overnutrition; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; post-partum bleeding; postpartum hemorrhage; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; purpura, thrombotic thrombocytopenic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; purpura, thrombotic thrombocytopenic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy-related first time venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy-related first time venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; pre-eclampsia; pregnancy complications, hematologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; pregnancy complications, hematologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
preeclampsia; hypertension, pregnancy induced; eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease preeclampsia; hypertension, pregnancy induced; eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral palsy; pregnancy complications, infectious; virus diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral palsy; pregnancy complications, infectious; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hiv infections; pregnancy complications, infectious; viremia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv infections; pregnancy complications, infectious; viremia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
multifetal pregnancy outcome. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease multifetal pregnancy outcome. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, cardiovascular; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, cardiovascular; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; pregnancy complications, hematologic; puerperal disorders; pulmonary embolism; thrombophilia; thrombophlebitis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vasodilation during pregnancy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vasodilation during pregnancy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; premature birth; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fetal growth retardation; periodontal diseases; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; periodontal diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications; prenatal exposure delayed effects Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
herpesviridae infections; kaposi sarcoma; pregnancy complications, infectious; sarcoma, kaposi Gene SetFrom GAD Gene-Disease Associations genes associated with the disease herpesviridae infections; kaposi sarcoma; pregnancy complications, infectious; sarcoma, kaposi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pre-eclampsia; pregnancy complications, hematologic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pre-eclampsia; pregnancy complications, hematologic 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. |
fetal growth retardation; intrauterine growth retardation; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; pregnancy complications, hematologic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy-induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depression, postpartum; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depression, postpartum; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abruptio placentae; placenta abruptio; pregnancy complications; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abruptio placentae; placenta abruptio; pregnancy complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, infectious; ureaplasma infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, infectious; ureaplasma infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy-associated venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy-associated venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bacterial vaginosis; fetal membranes, premature rupture; obstetric labor, premature; pregnancy complications, infectious; vaginosis, bacterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bacterial vaginosis; fetal membranes, premature rupture; obstetric labor, premature; pregnancy complications, infectious; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy-induced; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy-induced; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neural tube defects; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neural tube defects; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hepatitis c; pregnancy complications, infectious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hepatitis c; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
malaria, falciparum; parasitemia; placenta diseases; pregnancy complications, parasitic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease malaria, falciparum; parasitemia; placenta diseases; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic retinopathy; obstetric labor, premature; pre-eclampsia; pregnancy in diabetics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic retinopathy; obstetric labor, premature; pre-eclampsia; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
budd-chiari syndrome; pregnancy complications, hematologic; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease budd-chiari syndrome; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension, pregnancy induced Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension, pregnancy induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy complications, hematologic; thromboembolism; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy complications, hematologic; thromboembolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholestasis, intrahepatic; intrahepatic cholestasis; pregnancy complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholestasis, intrahepatic; intrahepatic cholestasis; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hiv seropositivity; pregnancy complications, infectious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hiv seropositivity; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term pregnancy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
female pregnancy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female pregnancy biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryonic process involved in female pregnancy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic process involved in female pregnancy biological process from the curated GO Biological Process Annotations 2015 dataset. |
maternal process involved in female pregnancy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the maternal process involved in female pregnancy biological process from the curated GO Biological Process Annotations 2015 dataset. |
mammary gland branching involved in pregnancy Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mammary gland branching involved in pregnancy biological process from the curated GO Biological Process Annotations 2015 dataset. |
Glycemic traits (pregnancy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Glycemic traits (pregnancy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
toxemia of pregnancy Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the toxemia of pregnancy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
increased serum bile acid concentration during pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the increased serum bile acid concentration during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal liver function tests during pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
toxemia of pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the toxemia of pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
maternal virilization in pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the maternal virilization in pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Pregnancy Complications, Infectious Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pregnancy Complications, Infectious phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pregnancy Complications, Hematologic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pregnancy Complications, Hematologic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pregnancy Complications, Parasitic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pregnancy Complications, Parasitic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pregnancy Complications Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pregnancy Complications phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pregnancy Complications, Neoplastic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pregnancy Complications, Neoplastic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hypertension, Pregnancy-Induced Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hypertension, Pregnancy-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pregnancy Complications, Cardiovascular Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pregnancy Complications, Cardiovascular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pregnancy, Ectopic Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pregnancy, Ectopic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Pregnancy in Diabetics Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Pregnancy in Diabetics phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Peptidase M43, pregnancy-associated plasma-A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase M43, pregnancy-associated plasma-A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
impaired mammary gland growth during pregnancy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the impaired mammary gland growth during pregnancy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pregnancy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pregnancy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mammary gland growth during pregnancy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mammary gland growth during pregnancy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pregnancy-related premature death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset. |
hellp syndrome, maternal, of pregnancy Gene SetFrom OMIM Gene-Disease Associations genes associated with the hellp syndrome, maternal, of pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset. |
cholestasis, intrahepatic, of pregnancy, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cholestasis, intrahepatic, of pregnancy, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cholestasis, intrahepatic, of pregnancy, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cholestasis, intrahepatic, of pregnancy, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hypertension, pregnancy-induced} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hypertension, pregnancy-induced} phenotype from the curated OMIM Gene-Disease Associations dataset. |
fatty liver, acute, of pregnancy Gene SetFrom OMIM Gene-Disease Associations genes associated with the fatty liver, acute, of pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset. |
pregnancy Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term pregnancy in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Abnormal Liver Function Tests During Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Liver Function Tests During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Intrahepatic Cholestasis Of Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Intrahepatic Cholestasis Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Toxemia Of Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Toxemia Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pregnancy Complications Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pregnancy Complications in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thyrotoxicosis In Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thyrotoxicosis In Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Fatty Liver Of Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Fatty Liver Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lchad Deficiency With Maternal Acute Fatty Liver Of Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lchad Deficiency With Maternal Acute Fatty Liver Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cancer And Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cancer And Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Impaired Glucose Tolerance In Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Impaired Glucose Tolerance In Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervical Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervical Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pregnancy Preterm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pregnancy Preterm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anti-D Isoimmunization Affecting Pregnancy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anti-D Isoimmunization Affecting Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Early Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pregnancy In Diabetics Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pregnancy In Diabetics in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Serum Bile Acid Concentration During Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Serum Bile Acid Concentration During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pregnancy Associated Hypertension Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pregnancy Associated Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ectopic Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ectopic Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pregnancy, Tubal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pregnancy, Tubal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Maternal Virilization In Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maternal Virilization In Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Maternal Fever In Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Maternal Fever In Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Transient Hypertension Of Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Transient Hypertension Of Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Alcohol Consumption During Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Alcohol Consumption During Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nausea In Pregnancy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nausea In Pregnancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal mammary gland growth during pregnancy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mammary gland growth during pregnancy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
pregnancy-related premature death Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pregnancy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pregnancy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired mammary gland growth during pregnancy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired mammary gland growth during pregnancy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
premature mammary gland growth during pregnancy Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the premature mammary gland growth during pregnancy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Mammary gland development pregnancy and lactation stage 3 of 4 Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Mammary gland development pregnancy and lactation stage 3 of 4 pathway from the WikiPathways Pathways 2024 dataset. |
Intrahepatic cholestasis of pregnancy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Intrahepatic cholestasis of pregnancy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Intrahepatic cholestasis of pregnancy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic cholestasis of pregnancy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ectopic pregnancy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ectopic pregnancy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intrahepatic cholestasis of pregnancy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic cholestasis of pregnancy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pregnancy adenoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pregnancy adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Intrahepatic cholestasis of pregnancy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrahepatic cholestasis of pregnancy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Abnormal liver function tests during pregnancy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal liver function tests during pregnancy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Adiponectin levels in pregnancy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adiponectin levels in pregnancy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Preterm birth (maternal effect) (maternal pre-pregnancy BMI interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Preterm birth (maternal effect) (maternal pre-pregnancy BMI interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Glycemic traits (pregnancy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glycemic traits (pregnancy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Fasting glucose in pregnancy (gestational week 14-16) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fasting glucose in pregnancy (gestational week 14-16) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Two-hour glucose in pregnancy (gestational week 30-32) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Two-hour glucose in pregnancy (gestational week 30-32) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
General glucose level in pregnancy (gestational week 30-32) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the General glucose level in pregnancy (gestational week 30-32) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Severity of nausea and vomiting of pregnancy Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severity of nausea and vomiting of pregnancy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Alloimmunization response to pregnancy (HLA class I) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Alloimmunization response to pregnancy (HLA class I) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Depression x maternal smoking during pregnancy interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Depression x maternal smoking during pregnancy interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Anxiety x maternal smoking during pregnancy interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anxiety x maternal smoking during pregnancy interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myoglobinuria, acute recurrent, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myoglobinuria, acute recurrent, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Benign recurrent intrahepatic cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Benign recurrent intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypotrichosis and recurrent skin vesicles Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hydatidiform mole, recurrent, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hydatidiform mole, recurrent, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
recurrent axon collateral Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the recurrent axon collateral cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Hypotrichosis And Recurrent Skin Vesicles Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 from the curated CTD Gene-Disease Associations dataset. |
CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 from the curated CTD Gene-Disease Associations dataset. |
Myoglobinuria, Acute Recurrent, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myoglobinuria, Acute Recurrent, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 from the curated CTD Gene-Disease Associations dataset. |
Vertigo, Benign Recurrent, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Vertigo, Benign Recurrent, 2 from the curated CTD Gene-Disease Associations dataset. |
recurrent corneal erosion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease recurrent corneal erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
recurrent hypersomnia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease recurrent hypersomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
idiopathic recurrent miscarriage. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriage. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent bacterial infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent bacterial infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
respiratory papillomatosis, juvenile-onset; recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease respiratory papillomatosis, juvenile-onset; recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
idiopathic recurrent miscarriages Gene SetFrom GAD Gene-Disease Associations genes associated with the disease idiopathic recurrent miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent cardiovascular event Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent cardiovascular event in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent spontaneous miscarriages Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent spontaneous miscarriages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent abortions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent abortions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent aphthous stomatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent aphthous stomatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spinal cord infarction and recurrent venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spinal cord infarction and recurrent venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent spontaneous abortion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent spontaneous abortion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent oral ulcers Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent oral ulcers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent deep-vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent deep-vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent or chronic idiopathic pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent or chronic idiopathic pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent acute pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent acute pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
herpes-associated recurrent lymphocytic meningitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease herpes-associated recurrent lymphocytic meningitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent respiratory infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent respiratory infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent respiratory papillomatosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent respiratory papillomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
recurrent Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term recurrent in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
recurrent hypersomnia Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease recurrent hypersomnia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
recurrent viral infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent viral infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent mycobacterial infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent mycobacterial infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent infection of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent mycobacterium avium complex infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent mycobacterium avium complex infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent bacterial infections Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the recurrent bacterial infections phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
recurrent aspergillus infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent aspergillus infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent abscess formation Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent abscess formation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent mandibular subluxations Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent mandibular subluxations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent fungal infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent fungal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent staphylococcal infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent staphylococcal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent pharyngitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent pharyngitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bacterial infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent vulvovaginal candidiasis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent vulvovaginal candidiasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bacterial meningitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bacterial meningitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent pneumonia Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent pneumonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infection of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infection of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent enteroviral infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent enteroviral infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent thrombophlebitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent thrombophlebitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent cerebral hemorrhage Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent cerebral hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent aspiration pneumonia Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent aspiration pneumonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent encephalopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent e. coli infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent e. coli infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent mycobacterial infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent mycobacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent aphthous stomatitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent aphthous stomatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent pancreatitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent pancreatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent lower respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections in infancy and early childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
severe recurrent varicella Gene SetFrom HPO Gene-Disease Associations genes associated with the severe recurrent varicella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent otitis media Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent otitis media phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent meningitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent meningitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent candida infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent candida infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent urinary tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent urinary tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
failure to thrive secondary to recurrent infections Gene SetFrom HPO Gene-Disease Associations genes associated with the failure to thrive secondary to recurrent infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent cutaneous abscess formation Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent cutaneous abscess formation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent upper and lower respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent upper and lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent burkholderia cepacia infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent burkholderia cepacia infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent spontaneous abortion Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent spontaneous abortion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent sinopulmonary infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent sinopulmonary infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent klebsiella infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent klebsiella infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent systemic pyogenic infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent systemic pyogenic infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent myoglobinuria Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent myoglobinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent gram-negative bacterial infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent gram-negative bacterial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent corneal erosions Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent corneal erosions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections due to aspiration Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent respiratory infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent respiratory infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spontaneous, recurrent epistaxis Gene SetFrom HPO Gene-Disease Associations genes associated with the spontaneous, recurrent epistaxis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent singultus Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent singultus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent subcortical infarcts Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent subcortical infarcts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent skin infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bronchopulmonary infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bronchopulmonary infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent mycobacterium avium complex infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent mycobacterium avium complex infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent hypoglycemia Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent protozoan infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent protozoan infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent upper respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent upper respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent meningococcal disease Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent meningococcal disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent viral infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent viral infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent sinusitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent sinusitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bacterial skin infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bacterial skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent serratia marcescens infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent serratia marcescens infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent streptococcus pneumoniae infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent streptococcus pneumoniae infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent neisserial infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent neisserial infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent deep vein thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent deep vein thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent opportunistic infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent opportunistic infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent bronchitis Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent bronchitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent haemophilus influenzae infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent haemophilus influenzae infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent cutaneous fungal infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent cutaneous fungal infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent staphylococcus aureus infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent staphylococcus aureus infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hydatidiform mole, recurrent, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydatidiform mole, recurrent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hydatidiform mole, recurrent, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hydatidiform mole, recurrent, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
t-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the t-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
?hypotrichosis and recurrent skin vesicles Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?hypotrichosis and recurrent skin vesicles phenotype from the curated OMIM Gene-Disease Associations dataset. |
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyper-ige recurrent infection syndrome, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyper-ige recurrent infection syndrome, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
invasive pneumococcal disease, recurrent isolated, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the invasive pneumococcal disease, recurrent isolated, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
invasive pneumococcal disease, recurrent isolated, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the invasive pneumococcal disease, recurrent isolated, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
cholestasis, benign recurrent intrahepatic Gene SetFrom OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, recurrent, with pressure palsies Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, recurrent, with pressure palsies phenotype from the curated OMIM Gene-Disease Associations dataset. |
myoglobinuria, acute recurrent, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the myoglobinuria, acute recurrent, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
pyogenic bacterial infections, recurrent, due to myd88 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the pyogenic bacterial infections, recurrent, due to myd88 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
cholestasis, benign recurrent intrahepatic, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the cholestasis, benign recurrent intrahepatic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyper-ige recurrent infection syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyper-ige recurrent infection syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
vertigo, benign recurrent, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the vertigo, benign recurrent, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Recurrent Otitis Media Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Otitis Media in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Acute Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Endometrial Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Endometrial Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Ovarian Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ovarian Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Benign Recurrent Intrahepatic Cholestasis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Benign Recurrent Intrahepatic Cholestasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chronic Myelogenous Leukemia, Bcr-Abl1 Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Aphthous Ulcer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Aphthous Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Hepatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Major Depressive Episodes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Major Depressive Episodes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Genital Herpes Simplex Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Genital Herpes Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Sinusitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Sinusitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Upper Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Upper Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Seizure Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Hand Flapping Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hand Flapping in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Hodgkin'S Lymphoma Transformed Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Hodgkin'S Lymphoma Transformed Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Recurrent Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Recurrent Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Herpes Simplex Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cervix Carcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cervix Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Locally Recurrent Malignant Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Locally Recurrent Malignant Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Glioblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pterygium Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pterygium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Brain Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Brain Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Adult Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Adult Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Hepatocellular Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Desmoid-Type Fibromatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Desmoid-Type Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pancreatitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pancreatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Cerebral Hemorrhage Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cerebral Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Optic Neuritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Optic Neuritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Depressive Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Depressive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Malignant Glioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Bronchitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bronchitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Ulcer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colorectal Cancer Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colorectal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Chronic Lymphoid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chronic Lymphoid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Follicular Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Follicular Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Non-Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Squamous Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Adult Acute Lymphoblastic Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Adult Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Medulloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Medulloblastoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Hemophagocytic Lymphohistiocytosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Hemophagocytic Lymphohistiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Acute Otitis Media Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Otitis Media in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Meningitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Respiratory Papillomatosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Respiratory Papillomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Peritonitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Peritonitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oesophageal Carcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oesophageal Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Laryngeal Squamous Cell Carcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Laryngeal Squamous Cell Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult T-Cell Lymphoma/Leukaemia Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult T-Cell Lymphoma/Leukaemia Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Diffuse Large B-Cell Lymphoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Large B-Cell Lymphoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lung Adenocarcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lung Adenocarcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Classic Hodgkin Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Ovarian Serous Adenocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Ovarian Serous Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Rhabdomyosarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Atypical Teratoid/Rhabdoid Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oropharyngeal Cancer Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oropharyngeal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Rectal Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Rectal Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Dedifferentiated Liposarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Dedifferentiated Liposarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Cell Lung Cancer Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Cell Lung Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Erosion Of Cornea Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Erosion Of Cornea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Epithelial Recurrent Erosion Dystrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Epithelial Recurrent Erosion Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Genetic Recurrent Myoglobinuria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Genetic Recurrent Myoglobinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Bacterial Meningitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bacterial Meningitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Aspiration Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Aspiration Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mesothelioma Malignant Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mesothelioma Malignant Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pyelonephritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pyelonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Varicella, Severe Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Varicella, Severe Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Respiratory Tract Infections Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Recurrent Major Depression Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Recurrent Major Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyper-Ige Recurrent Infection Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Head And Neck Squamous Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Head And Neck Squamous Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lung Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lung Carcinoma Cell Type Unspecified Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Carcinoma Cell Type Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Anal Cancer Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Anal Cancer Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Head And Neck Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Head And Neck Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Lung Non-Squamous Non-Small Cell Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Lung Non-Squamous Non-Small Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Infections Due To Aspiration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Infections Due To Aspiration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Larynx Carcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Larynx Carcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ewing'S Sarcoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ewing'S Sarcoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Infections Of The Middle Ear Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Infections Of The Middle Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infections, Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infections, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Herpes Simplex Infection Of Eye Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Infection Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Laryngeal Nerve Paralysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Laryngeal Nerve Paralysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Cushing Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cushing Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Subcortical Infarcts Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Subcortical Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Intrahepatic Cholangiocarcinoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intrahepatic Cholangiocarcinoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 2 (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 2 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Mouth Ulcers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Mouth Ulcers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Recurrent Pericarditis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Recurrent Pericarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Invasive Pneumococcal Disease, Recurrent Isolated, 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Invasive Pneumococcal Disease, Recurrent Isolated, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Craniopharyngioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Craniopharyngioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Proliferative Glomerulonephritis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Proliferative Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Pulmonary Embolism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Pulmonary Embolism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Myoglobinuria, Acute Recurrent, Autosomal Recessive Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Myoglobinuria, Acute Recurrent, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Systemic Pyogenic Infections Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Systemic Pyogenic Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Anaplastic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Childhood Anaplastic Astrocytoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Malignant Peripheral Nerve Sheath Tumor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Chordoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Chordoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Acute Myeloid Leukemia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Cystitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cystitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypersomnia, Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypersomnia, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Salivary Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Salivary Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B-Cell Small Lymphocytic Lymphoma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Small Lymphocytic Lymphoma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Biliary Tract Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Biliary Tract Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Cerebral Infarction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Cerebral Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Plasma Cell Myeloma Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Plasma Cell Myeloma Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Salivary Gland Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Salivary Gland Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Bacterial Pneumonia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Bacterial Pneumonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Metabolic Encephalomyopathic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Metabolic Encephalomyopathic Crises, Recurrent, With Rhabdomyolysis, Cardiac Arrhythmias, And Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Thyroid Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Thyroid Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Herpes Simplex Labialis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Herpes Simplex Labialis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Anaplastic Large Cell Lymphoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Anaplastic Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Respiratory Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Respiratory Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Tumor Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Fevers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Fevers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spontaneous, Recurrent Epistaxis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous, Recurrent Epistaxis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Bacterial Infection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bacterial Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Fungal Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Fungal Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Opportunistic Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Opportunistic Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Viral Infection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Viral Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Mandibular Subluxations Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mandibular Subluxations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Skin Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infection Of The Gastrointestinal Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infection Of The Gastrointestinal Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Upper And Lower Respiratory Tract Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Upper And Lower Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Lower Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Lower Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Singultus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Singultus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Spontaneous Abortion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Spontaneous Abortion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Sinopulmonary Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Sinopulmonary Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Cutaneous Abscess Formation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Cutaneous Abscess Formation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Enteroviral Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Enteroviral Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Meningococcal Disease Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Meningococcal Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Neisserial Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Neisserial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Failure To Thrive Secondary To Recurrent Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Failure To Thrive Secondary To Recurrent Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Abscess Formation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Abscess Formation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Candida Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Candida Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Gastroenteritis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Gastroenteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Haemophilus Influenzae Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Haemophilus Influenzae Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Streptococcus Pneumoniae Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Streptococcus Pneumoniae Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Bronchopulmonary Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bronchopulmonary Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Protozoan Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Protozoan Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Staphylococcus Aureus Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Staphylococcus Aureus Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Vulvovaginal Candidiasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Vulvovaginal Candidiasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Infections In Infancy And Early Childhood Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections In Infancy And Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Myoglobinuria, Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Myoglobinuria, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Encephalopathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Intrapulmonary Hemorrhage Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Intrapulmonary Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Bacterial Skin Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bacterial Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Headache Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Headache Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Aspergillus Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Aspergillus Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Burkholderia Cepacia Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Burkholderia Cepacia Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Klebsiella Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Klebsiella Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Serratia Marcescens Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Serratia Marcescens Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Mycobacterial Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mycobacterial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Paroxysmal Headache Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Paroxysmal Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Vomiting, Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vomiting, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Bronchiolitis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Bronchiolitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Thrombophlebitis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Thrombophlebitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Mycobacterium Avium Complex Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Mycobacterium Avium Complex Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Hypoglycemia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Hypoglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Thromboembolism Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Thromboembolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Viral Skin Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Viral Skin Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Staphylococcal Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Staphylococcal Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Gram-Negative Bacterial Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Gram-Negative Bacterial Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Pharyngitis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Pharyngitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Deep Vein Thrombosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Deep Vein Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Low Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Low Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Shingles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Shingles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic recurrent multifocal osteomyelitis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chronic recurrent multifocal osteomyelitis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Benign recurrent intrahepatic cholestasis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Benign recurrent intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hyper IgE recurrent infection syndrome 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hyper IgE recurrent infection syndrome 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Benign recurrent intrahepatic cholestasis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Benign recurrent intrahepatic cholestasis 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hyper IgE recurrent infection syndrome 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyper IgE recurrent infection syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Benign recurrent intrahepatic cholestasis 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Benign recurrent intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chronic recurrent multifocal osteomyelitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic recurrent multifocal osteomyelitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Recurrent hypersomnia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Recurrent hypersomnia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Recurrent corneal erosion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Recurrent corneal erosion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Epithelial recurrent erosion dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epithelial recurrent erosion dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hyper IgE recurrent infection syndrome 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyper IgE recurrent infection syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Recurrent axon collateral Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Recurrent axon collateral cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Recurrent fever Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent fever phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Benign recurrent intrahepatic cholestasis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Benign recurrent intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent subcortical infarcts Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent subcortical infarcts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hyper-IgE recurrent infection syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyper-IgE recurrent infection syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Epithelial recurrent erosion dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Epithelial recurrent erosion dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent pancreatitis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent pancreatitis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent infections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent infections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acute Recurrent Myoglobinuria Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute Recurrent Myoglobinuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent respiratory infections Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent respiratory infections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent encephalopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Recurrent Neisseria infections due to factor D deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent Neisseria infections due to factor D deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Otitis media (recurrent) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Otitis media (recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Otitis media (chronic/recurrent) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Otitis media (chronic/recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Broad depression or major depressive disorder (recurrent) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Broad depression or major depressive disorder (recurrent) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Recurrent major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrent major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Recurrent major depressive disorder x sex interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrent major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Schizophrenia, bipolar disorder or recurrent major depressive disorder Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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; 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
{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. |
?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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |