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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. |
abortion, habitual; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; activated protein c resistance; infertility, female; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; infertility, female; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; abortion, spontaneous; obstetric labor complications; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; abortion, spontaneous; obstetric labor complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; abortion, spontaneous Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; abortion, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; abortion, spontaneous; autoimmune diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; abortion, spontaneous; autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; infertility; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; infertility; thrombophilia 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. |
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. |
infertility, female; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chlamydia infections; genital diseases, female; infertility, female; inflammation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chlamydia infections; genital diseases, female; infertility, female; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Abortion, Habitual Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Abortion, Habitual from the curated CTD 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. |
abortion, habitual; hyperhomocysteinemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; venous thrombosis 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. |
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. |
abortion, habitual Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; activated protein c resistance; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; thrombosis 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. |
abortion, habitual; abruptio placentae; activated protein c resistance; placenta abruptio; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; abruptio placentae; activated protein c resistance; placenta abruptio; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; activated protein c resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; abruptio placentae; placenta abruptio Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; abruptio placentae; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, habitual; hyperhomocysteinemia; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, habitual; hyperhomocysteinemia; thrombosis 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, 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. |
Abortion, Habitual Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Abortion, Habitual phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Abortion, Habitual Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abortion, Habitual in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
alveolar bone loss; periodontal attachment loss; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
Infertility, Female Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Infertility, Female from the curated CTD Gene-Disease Associations dataset. |
infertility, female; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; ovarian failure, premature Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; ovarian failure, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anovulation; infertility, female; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anovulation; infertility, female; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
female infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease female infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chlamydia infections; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chlamydia infections; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chlamydia infections; fallopian tube diseases; infertility, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chlamydia infections; fallopian tube diseases; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
female infertility Gene SetFrom HPO Gene-Disease Associations genes associated with the female infertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Infertility, Female Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Infertility, Female phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
female infertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the female infertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Female Infertility Associated With Anovulation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Infertility Associated With Anovulation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Infertility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
female infertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the female infertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
female infertility Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the female infertility phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Female infertility of uterine origin Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female infertility of uterine origin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female infertility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Female infertility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Female infertility due to zona pellucida defect Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Female infertility due to zona pellucida defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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. |
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. |
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. |
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. |
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. |
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. |
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. |
pregnancy loss, recurrent; fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; hearing loss, high-frequency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, high-frequency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
fetal loss, late; pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fetal loss, late; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; hearing loss, sudden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
complete hearing loss; deafness; hearing impairment; hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
habitual Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term habitual in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Habitual Snoring Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Habitual Snoring in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Maximum habitual alcohol consumption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Maximum habitual alcohol consumption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Abortion, Spontaneous Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Abortion, Spontaneous from the curated CTD Gene-Disease Associations dataset. |
Abortion, Threatened Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Abortion, Threatened from the curated CTD Gene-Disease Associations dataset. |
abortion, spontaneous; premature birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
spontaneous abortion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease spontaneous abortion 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. |
abortion, spontaneous Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abortion, spontaneous; diabetes, gestational; gestational diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; diabetes, gestational; gestational diabetes mellitus 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. |
abortion, spontaneous; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; venous 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. |
abortion, spontaneous; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; thrombosis 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. |
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. |
abortion Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abortion in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
spontaneous abortion Gene SetFrom HPO Gene-Disease Associations genes associated with the spontaneous abortion 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. |
Abortion, Missed Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Abortion, Missed phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Abortion, Spontaneous Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Abortion, Spontaneous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Spontaneous Abortion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spontaneous Abortion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abortion, Tubal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abortion, Tubal 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. |
Threatened Abortion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Threatened Abortion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
HOXA2-22223247-E11.5 EMBRYO-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the HOXA2-22223247-E11.5 EMBRYO-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
embryo selection Gene SetFrom GAD Gene-Disease Associations genes associated with the disease embryo selection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
embryo Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term embryo in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
anterior/posterior axis specification, embryo Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryo development ending in birth or egg hatching Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryo implantation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryo implantation biological process from the curated GO Biological Process Annotations 2015 dataset. |
embryo development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryo development biological process from the curated GO Biological Process Annotations 2015 dataset. |
zygotic determination of anterior/posterior axis, embryo Gene SetFrom GO Biological Process Annotations 2015 genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations 2015 dataset. |
changes to dna methylation involved in embryo development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the changes to dna methylation involved in embryo development biological process from the curated GO Biological Process Annotations 2015 dataset. |
dna methylation involved in embryo development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dna methylation involved in embryo development biological process from the curated GO Biological Process Annotations 2015 dataset. |
abnormal embryo attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
partial embryonic lethality between somite formation and embryo turning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the partial embryonic lethality between somite formation and embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased embryo size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased embryo size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed embryo turning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed embryo implantation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed embryo implantation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
impaired embryo implantation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the impaired embryo implantation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
embryo tissue necrosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the embryo tissue necrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
embryonic lethality between somite formation and embryo turning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the embryonic lethality between somite formation and embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo apposition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo apposition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
complete embryonic lethality between somite formation and embryo turning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality between somite formation and embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo turning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo implantation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo implantation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased embryo size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased embryo size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased embryo weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased embryo weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal preimplantation embryo development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal preimplantation embryo development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal direction of embryo turning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal direction of embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
failure of initiation of embryo turning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the failure of initiation of embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased embryo weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased embryo weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
failure of embryo implantation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the failure of embryo implantation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
incomplete embryo turning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the incomplete embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
plant embryo Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue plant embryo from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
embryo Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue embryo from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
embryo Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue embryo in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
plant embryo Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue plant embryo in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
somatic embryo Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue somatic embryo in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
plant embryo Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue plant embryo in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
embryo Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue embryo in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Embryo Death Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Embryo Death in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Embryo Disintegration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Embryo Disintegration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Embryo Resorption Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Embryo Resorption in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
embryo development ending in birth or egg hatching Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2023 dataset. |
anterior/posterior axis specification, embryo Gene SetFrom GO Biological Process Annotations 2023 genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations 2023 dataset. |
DNA methylation involved in embryo development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the DNA methylation involved in embryo development biological process from the curated GO Biological Process Annotations 2023 dataset. |
zygotic determination of anterior/posterior axis, embryo Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations 2023 dataset. |
HOXA2-22223247-E11.5-EMBRYO-MOUSE Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the HOXA2-22223247-E11.5-EMBRYO-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
CHD4-35695185-NICBASALROOTGANGLIA-MOUSE-EMBRYO Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the CHD4-35695185-NICBASALROOTGANGLIA-MOUSE-EMBRYO transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
MBD3-35695185-NICBASALROOTGANGLIA-MOUSE-EMBRYO Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the MBD3-35695185-NICBASALROOTGANGLIA-MOUSE-EMBRYO transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
TFAP2A-35110662-HEPM-HUMAN-EMBRYO Gene SetFrom ChEA Transcription Factor Targets 2022 target genes of the TFAP2A-35110662-HEPM-HUMAN-EMBRYO transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset. |
decreased embryo size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased embryo size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
embryonic lethality between somite formation and embryo turning, complete penetrance Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality between somite formation and embryo turning, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
embryo tissue necrosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the embryo tissue necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
failure of initiation of embryo turning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of initiation of embryo turning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
incomplete embryo turning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the incomplete embryo turning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed embryo turning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed embryo turning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo turning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo turning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
failure of embryo implantation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of embryo implantation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal preimplantation embryo development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal preimplantation embryo development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired embryo implantation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired embryo implantation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo attachment Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo attachment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased embryo weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased embryo weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
embryonic lethality between somite formation and embryo turning, incomplete penetrance Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality between somite formation and embryo turning, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal direction of embryo turning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal direction of embryo turning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo implantation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo implantation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo apposition Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo apposition phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed embryo implantation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed embryo implantation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased embryo size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased embryo size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
embryonic lethality between somite formation and embryo turning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality between somite formation and embryo turning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased embryo weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased embryo weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
embryo tumor Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the embryo tumor phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
embryo cyst Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the embryo cyst phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
embryo phenotype Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the embryo phenotype phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal embryo size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal embryo turning Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal embryo turning phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal embryo development Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal embryo development phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Pre implantation embryo Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Pre implantation embryo pathway from the WikiPathways Pathways 2024 dataset. |
embryo development ending in birth or egg hatching Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryo development ending in birth or egg hatching biological process from the curated GO Biological Process Annotations 2025 dataset. |
anterior/posterior axis specification, embryo Gene SetFrom GO Biological Process Annotations 2025 genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations 2025 dataset. |
zygotic determination of anterior/posterior axis, embryo Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations 2025 dataset. |
Plant embryo Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Plant embryo in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Somatic embryo Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Somatic embryo in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Syncytial embryo sac Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Syncytial embryo sac in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Oocyte/zygote/embryo maturation arrest Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Oocyte/zygote/embryo maturation arrest phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
PMC6151027-12864_2018_5080_MOESM3_ESM.xlsx-Embryo-Hatchling_1272_AR-DEGs-Symbol_AR Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC6151027-12864_2018_5080_MOESM3_ESM.xlsx-Embryo-Hatchling_1272_AR-DEGs-Symbol_AR transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
Infertility associated with multi-tailed spermatozoa and excessive DNA Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
CATSPER-Related Male Infertility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the CATSPER-Related Male Infertility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infertility, Male Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Infertility, Male from the curated CTD Gene-Disease Associations dataset. |
Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa from the curated CTD Gene-Disease Associations dataset. |
Infertility Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Infertility from the curated CTD Gene-Disease Associations dataset. |
Deafness, Sensorineural, And Male Infertility Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Sensorineural, And Male Infertility from the curated CTD Gene-Disease Associations dataset. |
Infertility, Male Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Infertility, Male in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
male infertility Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease male infertility in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
male infertility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease male infertility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
infertility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease infertility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cystic fibrosis; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; urogenital abnormalities Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; urogenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; sex chromosome aberrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; oligospermia; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; oligospermia; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dna damage; infertility, male; varicocele Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dna damage; infertility, male; varicocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
idiopathic infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease idiopathic infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome deletion; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome deletion; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility; uterine diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility; uterine diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dna damage; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dna damage; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cryptorchidism; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cryptorchidism; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility; ovarian hyperstimulation syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility; ovarian hyperstimulation syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; neoplasms, prostatic; neoplasms, testis; prostatic neoplasms; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; neoplasms, prostatic; neoplasms, testis; prostatic neoplasms; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
asthenozoospermia; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease asthenozoospermia; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
testosterone; infertility, male; hypogonadism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease testosterone; infertility, male; hypogonadism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gonadal dysgenesis, 46,xy; infertility, male; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gonadal dysgenesis, 46,xy; infertility, male; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; varicocele Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; varicocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; hypospadias; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; hypospadias; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cystic fibrosis; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cystic fibrosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced trans-activation impaired sperm production and male infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced trans-activation impaired sperm production and male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
drug hypersensitivity; endometriosis; infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease drug hypersensitivity; endometriosis; infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
familial mediterranean fever; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial mediterranean fever; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, tubal factor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, tubal factor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
normogonadotropic anovulatory infertility Gene SetFrom GAD Gene-Disease Associations genes associated with the disease normogonadotropic anovulatory infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; sertoli cell-only syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; sertoli cell-only syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemochromatosis; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemochromatosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hernia, inguinal; infertility, male Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hernia, inguinal; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, male; oligospermia; sex chromosome aberrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term infertility in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Male infertility Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Male infertility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
male infertility Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease male infertility in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
male infertility Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the male infertility phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
infertility Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the infertility phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
infertility Gene SetFrom HPO Gene-Disease Associations genes associated with the infertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
male infertility Gene SetFrom HPO Gene-Disease Associations genes associated with the male infertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Infertility, Male Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Infertility, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Infertility Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Infertility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
infertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the infertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
male infertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the male infertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
?male infertility Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?male infertility phenotype from the curated OMIM Gene-Disease Associations dataset. |
deafness and male infertility Gene SetFrom OMIM Gene-Disease Associations genes associated with the deafness and male infertility phenotype from the curated OMIM Gene-Disease Associations dataset. |
?male infertility due to acrosin deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
Ovarian Infertility Genes(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Ovarian Infertility Genes(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Ovarian Infertility Genes(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Ovarian Infertility Genes(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
infertility Gene SetFrom PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease infertility from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset. |
Male Infertility With Teratozoospermia Due To Single Gene Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Infertility With Teratozoospermia Due To Single Gene Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Infertility With Large-Headed, Multiflagellar, Polyploid Spermatozoa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Infertility With Large-Headed, Multiflagellar, Polyploid Spermatozoa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Infertility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infertility Tubal Factor Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infertility Tubal Factor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Oligosynaptic Infertility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Oligosynaptic Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Male Infertility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Male Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Infertility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Male Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Infertility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Infertility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
infertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the infertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
male infertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the male infertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
male infertility Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the male infertility phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Ovarian infertility Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Ovarian infertility pathway from the WikiPathways Pathways 2024 dataset. |
Male infertility Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Male infertility pathway from the WikiPathways Pathways 2024 dataset. |
Male infertility Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Male infertility from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Male infertility due to globozoospermia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Male infertility due to globozoospermia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Male infertility Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Male infertility in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male infertility due to globozoospermia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility due to globozoospermia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Infertility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infertility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male infertility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Male infertility due to acephalic spermatozoa Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Male infertility due to acephalic spermatozoa in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Infertility disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infertility disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Male infertility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Male infertility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Infertility associated Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Infertility associated phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Oligosynaptic infertility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Oligosynaptic infertility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Deafness-infertility syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Deafness-infertility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Male infertility due to gonadal dysgenesis or sperm disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Male infertility due to gonadal dysgenesis or sperm disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Male infertility Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Male infertility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
female germ cell nucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the female germ cell nucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
female pronucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the female pronucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
female germline ring canal Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female germline ring canal cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
female germline ring canal inner rim Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female germline ring canal inner rim cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
female germ cell nucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female germ cell nucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
female pronucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the female pronucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Genital Neoplasms, Female Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genital Neoplasms, Female from the curated CTD Gene-Disease Associations dataset. |
Epilepsy, Female-Restricted, with Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Female-Restricted, with Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Female Urogenital Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Female Urogenital Diseases from the curated CTD Gene-Disease Associations dataset. |
Genital Diseases, Female Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Genital Diseases, Female from the curated CTD Gene-Disease Associations dataset. |
female reproductive system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease female reproductive system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
female reproductive organ cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease female reproductive organ cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
female reproductive organ benign neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease female reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
female reproductive system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease female reproductive system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
female urethral cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female urethral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female breast cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female breast cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female stress incontinence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female stress incontinence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female reproductive system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female reproductive organ cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive organ cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female breast carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female breast carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female reproductive organ benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
prolapse of female genital organ Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease prolapse of female genital organ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female reproductive endometrioid cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease female reproductive endometrioid cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
female preferences for male odors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease female preferences for male odors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chlamydia infections; genital diseases, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chlamydia infections; genital diseases, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postnatal female survival Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postnatal female survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genital diseases, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genital diseases, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
genital neoplasms, female Gene SetFrom GAD Gene-Disease Associations genes associated with the disease genital neoplasms, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
female pseudohermaphroditism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease female pseudohermaphroditism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
male-to-female transsexualism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease male-to-female transsexualism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
female Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term female in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
development of primary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2015 genes participating in the development of primary female sexual characteristics biological process from the curated GO Biological Process Annotations 2015 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. |
female meiosis sister chromatid cohesion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female meiosis sister chromatid cohesion biological process from the curated GO Biological Process Annotations 2015 dataset. |
female pronucleus assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female pronucleus assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
female meiosis i Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female meiosis i 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. |
female gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
female somatic sex determination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female somatic sex determination biological process from the curated GO Biological Process Annotations 2015 dataset. |
female meiotic division Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female meiotic division biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of female receptivity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of female receptivity biological process from the curated GO Biological Process Annotations 2015 dataset. |
female genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
female mating behavior Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female mating behavior biological process from the curated GO Biological Process Annotations 2015 dataset. |
development of secondary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2015 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of female gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
female courtship behavior Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female courtship behavior biological process from the curated GO Biological Process Annotations 2015 dataset. |
protection of dna demethylation of female pronucleus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protection of dna demethylation of female pronucleus biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of female gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
female meiosis ii Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female meiosis ii biological process from the curated GO Biological Process Annotations 2015 dataset. |
spindle assembly involved in female meiosis i Gene SetFrom GO Biological Process Annotations 2015 genes participating in the spindle assembly involved in female meiosis i biological process from the curated GO Biological Process Annotations 2015 dataset. |
female genitalia development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female genitalia development biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of female receptivity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of female receptivity biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of female receptivity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of female receptivity biological process from the curated GO Biological Process Annotations 2015 dataset. |
female gamete generation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female gamete generation biological process from the curated GO Biological Process Annotations 2015 dataset. |
female sex determination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the female sex determination biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of female gonad development biological process from the curated GO Biological Process Annotations 2015 dataset. |
spindle assembly involved in female meiosis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the spindle assembly involved in female meiosis biological process from the curated GO Biological Process Annotations 2015 dataset. |
female germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the female germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
female pronucleus Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the female pronucleus cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
Sexual dysfunction (female) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
prolapse of female genital organ Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease prolapse of female genital organ in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
female breast cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease female breast cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
female reproductive organ cancer Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease female reproductive organ cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
female reproductive organ benign neoplasm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease female reproductive organ benign neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
female reproductive system disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease female reproductive system disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of female internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the female genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hypoplastic female external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplastic female external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
female hypogonadism Gene SetFrom HPO Gene-Disease Associations genes associated with the female hypogonadism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of female external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of female external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ambiguous genitalia, female Gene SetFrom HPO Gene-Disease Associations genes associated with the ambiguous genitalia, female phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of female internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of female internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the female genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the female genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
female external genitalia in individual with 46,xy karyotype Gene SetFrom HPO Gene-Disease Associations genes associated with the female external genitalia in individual with 46,xy karyotype phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
female pseudohermaphroditism Gene SetFrom HPO Gene-Disease Associations genes associated with the female pseudohermaphroditism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Genital Neoplasms, Female Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Neoplasms, Female phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Genital Diseases, Female Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Genital Diseases, Female phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Meiosis arrest female protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Meiosis arrest female protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal female genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female meiosis i arrest Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female meiosis i arrest phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
female preputial gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal internal female genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal internal female genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced female fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced female fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female meiosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent external female genitalia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent external female genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female germ cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female germ cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed female fertility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed female fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent internal female genitalia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent internal female genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external female genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external female genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female preputial gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female preputial gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal female reproductive gland morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[analgesia from kappa-opioid receptor agonist, female-specific] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [analgesia from kappa-opioid receptor agonist, female-specific] phenotype from the curated OMIM Gene-Disease Associations dataset. |
luteinizing hormone resistance, female Gene SetFrom OMIM Gene-Disease Associations genes associated with the luteinizing hormone resistance, female phenotype from the curated OMIM Gene-Disease Associations dataset. |
female Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term female in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01508 Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Female RO_01508 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01549 Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Female RO_01549 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01480 Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Female RO_01480 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01536 Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Female RO_01536 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Skeletal Muscle Female Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Skeletal Muscle Female relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
female reproductive gland Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female reproductive gland from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
female reproductive system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female reproductive system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
internal female genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
female pudendum Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female pudendum from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
external female genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue external female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
female reproductive system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female reproductive system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
female reproductive gland Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue female reproductive gland in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
internal female genital organ Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue internal female genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset. |
female reproductive gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female reproductive gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
internal female genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue internal female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
female reproductive system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female reproductive system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
female cone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
female urethra Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female urethra in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
external female genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue external female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
female pudendum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue female pudendum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Female Breast Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Breast Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Subfertility, Female Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Subfertility, Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Hypogonadism Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Hypogonadism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Female Reproductive System Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Female Reproductive System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Secondary Malignant Neoplasm Of Female Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Female Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Female External Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Female External Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Infiltrating Duct Carcinoma Of Female Breast Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Infiltrating Duct Carcinoma Of Female Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
46, Xy Female Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease 46, Xy Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Pseudohermaphroditism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Pseudohermaphroditism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Sexual Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Pseudo-Turner Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Pseudo-Turner Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Female Internal Genitalia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Female Internal Genitalia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cystocele (Female) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cystocele (Female) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dyspareunia (Female) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dyspareunia (Female) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Anorgasmia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Anorgasmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ambiguous Genitalia, Female Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ambiguous Genitalia, Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Athlete Triad Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Athlete Triad Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Luteinizing Hormone Resistance, Female Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Luteinizing Hormone Resistance, Female in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Increased Analgesia From Kappa-Opioid Receptor Agonist, Female-Specific (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Increased Analgesia From Kappa-Opioid Receptor Agonist, Female-Specific (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Stress Incontinence Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Stress Incontinence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Precocious Female Puberty Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Precocious Female Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Pattern Alopecia (Disorder) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Pattern Alopecia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Breast Pain Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Breast Pain Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chronic Pelvic Pain Of Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chronic Pelvic Pain Of Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Female Sterility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Sterility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Female Libido Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Female Libido in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Female Libido Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Female Libido in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pelvic Pain Female Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pelvic Pain Female in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Female External Genitalia In Individual With 46,Xy Karyotype Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female External Genitalia In Individual With 46,Xy Karyotype in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Female Virilization Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Virilization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Female Puberty Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Female Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Female Puberty Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Female Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
female gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
female meiosis I Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female meiosis I biological process from the curated GO Biological Process Annotations 2023 dataset. |
female genitalia development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female genitalia development biological process from the curated GO Biological Process Annotations 2023 dataset. |
female gamete generation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female gamete generation biological process from the curated GO Biological Process Annotations 2023 dataset. |
female genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the female genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of female gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
development of primary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2023 genes participating in the development of primary female sexual characteristics biological process from the curated GO Biological Process Annotations 2023 dataset. |
development of secondary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2023 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of female gonad development biological process from the curated GO Biological Process Annotations 2023 dataset. |
female pronucleus Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the female pronucleus cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
female germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the female germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
abnormal female germ cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female germ cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced female fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female meiosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female meiosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female reproductive system morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female reproductive system morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased aggression towards female mice Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased aggression towards female mice phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired sperm migration in female genital tract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired sperm migration in female genital tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ambiguous external female genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ambiguous external female genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent internal female genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent internal female genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female reproductive system physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female reproductive system physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed female fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent external female genitalia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent external female genitalia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female meiosis I arrest Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female meiosis I arrest phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased female germ cell apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased female germ cell apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal internal female genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal female genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal external female genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal external female genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female urethra morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female urethra morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent female preputial gland Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent female preputial gland phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
female preputial gland hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enhanced female fertility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enhanced female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female genitalia morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female genitalia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sperm migration in female genital tract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm migration in female genital tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal female germ cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal female germ cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Female steroid hormones in cardiomyocyte energy metabolism Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Female steroid hormones in cardiomyocyte energy metabolism pathway from the WikiPathways Pathways 2024 dataset. |
female meiosis chromosome segregation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female meiosis chromosome segregation biological process from the curated GO Biological Process Annotations 2025 dataset. |
female gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
female meiosis I Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female meiosis I biological process from the curated GO Biological Process Annotations 2025 dataset. |
female meiotic nuclear division Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female meiotic nuclear division biological process from the curated GO Biological Process Annotations 2025 dataset. |
female genitalia development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female genitalia development biological process from the curated GO Biological Process Annotations 2025 dataset. |
female gamete generation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female gamete generation biological process from the curated GO Biological Process Annotations 2025 dataset. |
female genitalia morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female genitalia morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
female pronucleus assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the female pronucleus assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of female gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
epigenetic programing of female pronucleus Gene SetFrom GO Biological Process Annotations 2025 genes participating in the epigenetic programing of female pronucleus biological process from the curated GO Biological Process Annotations 2025 dataset. |
spindle assembly involved in female meiosis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the spindle assembly involved in female meiosis biological process from the curated GO Biological Process Annotations 2025 dataset. |
development of primary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2025 genes participating in the development of primary female sexual characteristics biological process from the curated GO Biological Process Annotations 2025 dataset. |
development of secondary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2025 genes participating in the development of secondary female sexual characteristics biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of female gonad development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of female gonad development biological process from the curated GO Biological Process Annotations 2025 dataset. |
female pronucleus Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the female pronucleus cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
female germ cell nucleus Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the female germ cell nucleus cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Female reproductive system disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Female reproductive system disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Female reproductive organ cancer Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Female reproductive organ cancer from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Female reproductive system disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Female reproductive system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive organ cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Female reproductive organ cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive organ benign neoplasm Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Female reproductive organ benign neoplasm in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive organ cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive organ cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive system disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female breast carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female breast carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive organ benign neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female breast cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female breast cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive endometrioid cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female reproductive endometrioid cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Prolapse of female genital organ Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Prolapse of female genital organ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female urethral cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female urethral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female stress incontinence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female stress incontinence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inhibited female orgasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inhibited female orgasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
female-restricted syndromic X-linked intellectual disability 99 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease female-restricted syndromic X-linked intellectual disability 99 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female breast nipple and areola cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Female breast nipple and areola cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Female reproductive gland Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female reproductive gland from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive system Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female reproductive system from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal female genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
External female genital organ Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue External female genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Female pudendum Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female pudendum from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive system Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female reproductive system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive gland Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Female reproductive gland in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal female genital organ Gene SetFrom TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Internal female genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female reproductive gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female reproductive system Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female reproductive system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Internal female genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Internal female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female pudendum Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female pudendum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
External female genital organ Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue External female genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female accessory gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female accessory gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female inflorescence Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female inflorescence in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female urethra Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female urethra in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female cone Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Female cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Female pronucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Female pronucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Female germ cell nucleus Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Female germ cell nucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Female germ cell nucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Female germ cell nucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Female pronucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Female pronucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Female germline ring canal Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Female germline ring canal cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Facial attractiveness (female raters) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Facial attractiveness (female raters) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sexual dysfunction (female) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (female) 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. |
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. |
pregnancy loss, second trimester Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, second trimester in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, central Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, central in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autosomal dominant hearing loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autosomal dominant hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
hearing loss, sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; weight gain; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; weight gain; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
h-ras allele loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease h-ras allele loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; coagulation disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; rhinitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sensorineural nonsyndromic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sensorineural nonsyndromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
goiter; hearing loss, sensorineural Gene SetFrom GAD Gene-Disease Associations genes associated with the disease goiter; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood loss, surgical Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood loss, surgical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
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. |
pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycystic ovary syndrome; pregnancy loss, recurrent Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycystic ovary syndrome; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, sudden Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pregnancy loss, recurrent; in vitro fertilization success Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; in vitro fertilization success in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
recurrent early fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent early fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
recurrent fetal loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced intrapartum blood loss--a possible evolutionary selection mechanism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced intrapartum blood loss--a possible evolutionary selection mechanism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hearing loss, bilateral Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hearing loss, bilateral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatty liver; insulin resistance; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatty liver; insulin resistance; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
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. |
pregnancy loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pregnancy loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lumen loss, late Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lumen loss, late in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
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. |
recurrent pregnancy loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease recurrent pregnancy loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
loss Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term loss in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of water loss via skin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of water loss via skin biological process from the curated GO Biological Process Annotations 2015 dataset. |
Weight loss (gastric bypass surgery) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Weight loss (gastric bypass surgery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
weight loss Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the weight loss phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
loss of ability to walk Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of ability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of ability to walk in first decade Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of ability to walk in first decade phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low-frequency hearing loss Gene SetFrom HPO Gene-Disease Associations genes associated with the low-frequency hearing loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of facial expression Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature loss of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the premature loss of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of voice Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of voice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of subcutaneous adipose tissue in limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of subcutaneous adipose tissue in limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent loss of toenails and fingernails Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent loss of toenails and fingernails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weight loss Gene SetFrom HPO Gene-Disease Associations genes associated with the weight loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of truncal subcutaneous adipose tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of truncal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
axonal loss Gene SetFrom HPO Gene-Disease Associations genes associated with the axonal loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scalp hair loss Gene SetFrom HPO Gene-Disease Associations genes associated with the scalp hair loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sudden central visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the sudden central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive central visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cranial nerve motor loss Gene SetFrom HPO Gene-Disease Associations genes associated with the cranial nerve motor loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of speech Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of speech phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
nonprogressive visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the nonprogressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neuronal loss in the cerebral cortex Gene SetFrom HPO Gene-Disease Associations genes associated with the neuronal loss in the cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neuronal loss in basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the neuronal loss in basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature loss of permanent teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the premature loss of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature loss of primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the premature loss of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal cord posterior columns myelin loss Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal cord posterior columns myelin loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of ability to walk in early childhood Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of consciousness Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of consciousness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neuronal loss in central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the neuronal loss in central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of facial adipose tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of facial adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral visual field loss Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral visual field loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of gluteal subcutaneous adipose tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of gluteal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory loss of all modalities Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive visual loss Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
loss of purkinje cells in the cerebellar vermis Gene SetFrom HPO Gene-Disease Associations genes associated with the loss of purkinje cells in the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adipose tissue loss Gene SetFrom HPO Gene-Disease Associations genes associated with the adipose tissue loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Blood Loss, Surgical Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Blood Loss, Surgical phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Central Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Tooth Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Unilateral Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Unilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Functional Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Functional phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Sensorineural Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Weight Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Weight Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Mixed Conductive-Sensorineural Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Mixed Conductive-Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Bilateral Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Bilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Noise-Induced Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Noise-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, High-Frequency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, High-Frequency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Periodontal Attachment Loss Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Periodontal Attachment Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hearing Loss, Sudden Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hearing Loss, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
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. |
{pregnancy loss, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset. |
?split-hand/foot malformation 1 with sensorineural hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 1} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{bulimia nervosa, age of onset of weight loss in} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {bulimia nervosa, age of onset of weight loss in} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{?hearing loss, cisplatin-induced, susceptibility to} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {?hearing loss, cisplatin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset. |
polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene SetFrom OMIM Gene-Disease Associations genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset. |
ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
congenital cataracts, hearing loss, and neurodegeneration Gene SetFrom OMIM Gene-Disease Associations genes associated with the congenital cataracts, hearing loss, and neurodegeneration phenotype from the curated OMIM Gene-Disease Associations dataset. |
{pregnancy loss, recurrent, susceptibility to, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {pregnancy loss, recurrent, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
Loss of Function of SMAD4 in Cancer Gene Setproteins participating in the Loss of Function of SMAD4 in Cancer pathway from the Reactome Pathways dataset. |
Loss of Function of TGFBR2 in Cancer Gene Setproteins participating in the Loss of Function of TGFBR2 in Cancer pathway from the Reactome Pathways dataset. |
Loss of Nlp from mitotic centrosomes Gene Setproteins participating in the Loss of Nlp from mitotic centrosomes pathway from the Reactome Pathways dataset. |
Loss of Function of TGFBR1 in Cancer Gene Setproteins participating in the Loss of Function of TGFBR1 in Cancer pathway from the Reactome Pathways dataset. |
Loss of proteins required for interphase microtubule organization from the centrosome Gene Setproteins participating in the Loss of proteins required for interphase microtubule organization from the centrosome pathway from the Reactome Pathways dataset. |
Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling Gene Setproteins participating in the Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling pathway from the Reactome Pathways dataset. |
Loss of Function of SMAD2/3 in Cancer Gene Setproteins participating in the Loss of Function of SMAD2/3 in Cancer pathway from the Reactome Pathways dataset. |
Sensorineural Hearing Loss (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Hearing Loss (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Conductive Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Conductive Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
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. |
Pregnancy Loss, Recurrent Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pregnancy Loss, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bilateral Sensory Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Sensory Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Hearing Loss Stapes Fixation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Hearing Loss Stapes Fixation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recessive Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recessive Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Nonscarring Hair Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Nonscarring Hair Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Volume Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Volume Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Corneal Epithelial Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Corneal Epithelial Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loss Of Skin Elasticity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Loss Of Skin Elasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loss Of Cervical Lordosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Loss Of Cervical Lordosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Paragangliomas With Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Paragangliomas With Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Cataracts, Hearing Loss, And Neurodegeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cataracts, Hearing Loss, And Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loss Of Speech Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Speech in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unspecified Visual Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unspecified Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Early Pregnancy Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Pregnancy Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Memory Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Memory Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Ability To Walk Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Visual Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neuronal Loss In Central Nervous System Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Axonal Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Visual Field Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Visual Field Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Subcutaneous Adipose Tissue In Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Subcutaneous Adipose Tissue In Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sudden Loss Of Visual Acuity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Loss Of Visual Acuity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Complete Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Premature Loss Of Permanent Teeth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Loss Of Permanent Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pregnancy Loss, Recurrent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pregnancy Loss, Recurrent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Memory Ability Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Memory Ability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Purkinje Cells In The Cerebellar Vermis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Purkinje Cells In The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spinal Cord Posterior Columns Myelin Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Cord Posterior Columns Myelin Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
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. |
Foveal Photoreceptor Outer Segment Loss On Macular Oct Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foveal Photoreceptor Outer Segment Loss On Macular Oct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Photoreceptor Layer Loss On Macular Oct Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Photoreceptor Layer Loss On Macular Oct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nail Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nail Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Facial Expression Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Facial Expression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neuronal Loss In Basal Ganglia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuronal Loss In Basal Ganglia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Adipose Tissue Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adipose Tissue Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Loss Of Toenails And Fingernails Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Loss Of Toenails And Fingernails in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Truncal Subcutaneous Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Truncal Subcutaneous Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Subcutaneous Adipose Tissue From Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Subcutaneous Adipose Tissue From Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Loss Of Facial Adipose Tissue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Loss Of Facial Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Ability To Walk In First Decade Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk In First Decade in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nonprogressive Visual Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonprogressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sudden Visual Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sudden Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Proprioception Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Proprioception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pre-Ictal Memory Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pre-Ictal Memory Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Retrograde Memory Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retrograde Memory Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Nonsyndromic Sensorineural Hearing Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonsyndromic Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cranial Nerve Motor Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cranial Nerve Motor Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
weight loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the weight loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of eyelid cilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of eyelid cilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
premature hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the premature hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to noise-induced hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of dopaminergic neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of dopaminergic neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
sensorineural hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the sensorineural hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
proximal convoluted tubule brush border loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
partial loss of secondary muscle spindle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of hippocampal neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of hippocampal neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to weight loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to weight loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to age-related hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to age-related hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
nonsyndromic hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the nonsyndromic hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
progressive hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
conductive hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the conductive hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in head/neck region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in head/neck region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal dorsal hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of glutamate neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of glutamate neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased susceptibility to ototoxicity-induced hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to ototoxicity-induced hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
syndromic hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the syndromic hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to noise-induced hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of basal ganglia neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of basal ganglia neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of cortex neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of cortex neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of GABAergic neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of GABAergic neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal susceptibility to hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal susceptibility to hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
loss of vibrissae Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the loss of vibrissae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased susceptibility to weight loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to weight loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed suckling reflex loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed suckling reflex loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
mixed hearing loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the mixed hearing loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in abdominal region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in abdominal region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
premature suckling reflex loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the premature suckling reflex loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in thorax region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in thorax region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Defective DNA double strand break response due to BARD1 loss of function Gene Setproteins participating in the Defective DNA double strand break response due to BARD1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective DNA double strand break response due to BRCA1 loss of function Gene Setproteins participating in the Defective DNA double strand break response due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function Gene Setproteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function pathway from the Reactome Pathways 2024 dataset. |
Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function Gene Setproteins participating in the Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function pathway from the Reactome Pathways 2024 dataset. |
Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function Gene Setproteins participating in the Defective Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to BRCA1 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to BRCA1 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to BRCA2 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to BRCA2 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective homologous recombination repair (HRR) due to PALB2 loss of function Gene Setproteins participating in the Defective homologous recombination repair (HRR) due to PALB2 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to ABCA4 loss of function Gene Setproteins participating in the Defective visual phototransduction due to ABCA4 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to LRAT loss of function Gene Setproteins participating in the Defective visual phototransduction due to LRAT loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1LW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1LW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1MW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1MW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to OPN1SW loss of function Gene Setproteins participating in the Defective visual phototransduction due to OPN1SW loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to RDH12 loss of function Gene Setproteins participating in the Defective visual phototransduction due to RDH12 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to RDH5 loss of function Gene Setproteins participating in the Defective visual phototransduction due to RDH5 loss of function pathway from the Reactome Pathways 2024 dataset. |
Defective visual phototransduction due to STRA6 loss of function Gene Setproteins participating in the Defective visual phototransduction due to STRA6 loss of function pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling Gene Setproteins participating in the Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of SMAD2/3 in Cancer Gene Setproteins participating in the Loss of Function of SMAD2/3 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of SMAD4 in Cancer Gene Setproteins participating in the Loss of Function of SMAD4 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of TGFBR1 in Cancer Gene Setproteins participating in the Loss of Function of TGFBR1 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of TGFBR2 in Cancer Gene Setproteins participating in the Loss of Function of TGFBR2 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of Function of TP53 in Cancer Gene Setproteins participating in the Loss of Function of TP53 in Cancer pathway from the Reactome Pathways 2024 dataset. |
Loss of MECP2 binding ability to 5hmC-DNA Gene Setproteins participating in the Loss of MECP2 binding ability to 5hmC-DNA pathway from the Reactome Pathways 2024 dataset. |
Loss of MECP2 binding ability to 5mC-DNA Gene Setproteins participating in the Loss of MECP2 binding ability to 5mC-DNA pathway from the Reactome Pathways 2024 dataset. |
Loss of MECP2 binding ability to the NCoR/SMRT complex Gene Setproteins participating in the Loss of MECP2 binding ability to the NCoR/SMRT complex pathway from the Reactome Pathways 2024 dataset. |
Loss of Nlp from mitotic centrosomes Gene Setproteins participating in the Loss of Nlp from mitotic centrosomes pathway from the Reactome Pathways 2024 dataset. |
Loss of function of MECP2 in Rett syndrome Gene Setproteins participating in the Loss of function of MECP2 in Rett syndrome pathway from the Reactome Pathways 2024 dataset. |
Loss of phosphorylation of MECP2 at T308 Gene Setproteins participating in the Loss of phosphorylation of MECP2 at T308 pathway from the Reactome Pathways 2024 dataset. |
Loss of proteins required for interphase microtubule organization from the centrosome Gene Setproteins participating in the Loss of proteins required for interphase microtubule organization from the centrosome pathway from the Reactome Pathways 2024 dataset. |
Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD Gene Setproteins participating in the Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD pathway from the Reactome Pathways 2024 dataset. |
Loss-of-function mutations in DBT cause MSUD2 Gene Setproteins participating in the Loss-of-function mutations in DBT cause MSUD2 pathway from the Reactome Pathways 2024 dataset. |
Loss-of-function mutations in DLD cause MSUD3/DLDD Gene Setproteins participating in the Loss-of-function mutations in DLD cause MSUD3/DLDD pathway from the Reactome Pathways 2024 dataset. |
PTEN Loss of Function in Cancer Gene Setproteins participating in the PTEN Loss of Function in Cancer pathway from the Reactome Pathways 2024 dataset. |
RAS signaling downstream of NF1 loss-of-function variants Gene Setproteins participating in the RAS signaling downstream of NF1 loss-of-function variants pathway from the Reactome Pathways 2024 dataset. |
Sensorineural hearing loss Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sensorineural hearing loss in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sensorineural hearing loss Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensorineural hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
drug-induced hearing loss Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease drug-induced hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Split hand-foot malformation 1 with sensorineural hearing loss Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Split hand-foot malformation 1 with sensorineural hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
camptodactyly-tall stature-scoliosis-hearing loss syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease camptodactyly-tall stature-scoliosis-hearing loss syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Short stature, hearing loss, retinitis pigmentosa, and distinctive facies Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Short stature, hearing loss, retinitis pigmentosa, and distinctive facies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive nonsyndromic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive nonsyndromic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pregnancy loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pregnancy loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sensorineural hearing loss disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensorineural hearing loss disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant nonsyndromic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant nonsyndromic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nonsyndromic genetic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonsyndromic genetic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Childhood onset hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked mixed hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked mixed hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary hearing loss and deafness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary hearing loss and deafness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral visual field loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral visual field loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Camptodactyly-tall stature-scoliosis-hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Camptodactyly-tall stature-scoliosis-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant keratitis-ichthyosis-hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant keratitis-ichthyosis-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nonsyndromic Hearing Loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonsyndromic Hearing Loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nonsyndromic sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonsyndromic sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Visual loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Noise induced hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Noise induced hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Loss of ambulation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Loss of ambulation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hearing loss and Retinal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hearing loss and Retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked nonsyndromic hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked nonsyndromic hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cone-rod dystrophy and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cone-rod dystrophy and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hearing loss in noise exposure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hearing loss in noise exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Trans-epidermal water loss Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Trans-epidermal water loss phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mosaic loss of chromosome Y (Y chromosome dosage) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mosaic loss of chromosome Y (Y chromosome dosage) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Weight loss (gastric bypass surgery) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Weight loss (gastric bypass surgery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mosaic loss of chromosome Y Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mosaic loss of chromosome Y phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hearing loss in Charcot-Marie-Tooth disease 1A Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hearing loss in Charcot-Marie-Tooth disease 1A phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cisplatin-induced hearing loss in childhood cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cisplatin-induced hearing loss in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |