Female Pseudo-Turner Syndrome

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Results for "Female Pseudo-Turner Syndrome": 1001 gene sets

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Female Pseudo-Turner Syndrome Gene Set From 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.
chlamydia infections; genital diseases, female; infertility, female; inflammation Gene Set From 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.
pseudo-torch syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pseudo-torch syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
Pseudo-Torch Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudo-Torch Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudo-Bartter Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudo-Bartter Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudo-Zellweger Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudo-Zellweger Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
pseudo-TORCH syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease pseudo-TORCH syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neonatal pseudo-hydrocephalic progeroid syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal pseudo-hydrocephalic progeroid syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pseudo-TORCH syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pseudo-TORCH syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From 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.
infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From 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.
Pseudo von Willebrand disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudo-Hurler polydystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudo-Hurler polydystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
intestinal pseudo-obstruction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease intestinal pseudo-obstruction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
colonic pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease colonic pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intestinal pseudo-obstruction; mitochondrial diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease intestinal pseudo-obstruction; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pseudo Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term pseudo in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
intestinal pseudo-obstruction Gene Set From HPO Gene-Disease Associations genes associated with the intestinal pseudo-obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Intestinal Pseudo-Obstruction Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Intestinal Pseudo-Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Smaug, pseudo-HEAT analogous topology Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Smaug, pseudo-HEAT analogous topology protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Chronic Intestinal Pseudo-Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Intestinal Pseudo-Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intestinal Pseudo-Obstruction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intestinal Pseudo-Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudo-Fractures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudo-Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudo-Hurler Polydystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pseudo-Hurler Polydystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pseudo Pelger-Huet Anomaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pseudo Pelger-Huet Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intestinal pseudo-obstruction Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Intestinal pseudo-obstruction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Colonic pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Colonic pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked chronic idiopathic intestinal pseudo-obstruction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked chronic idiopathic intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pseudo-Hurler polydystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pseudo-Hurler polydystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pseudo von Willebrand disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pseudo von Willebrand disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intestinal pseudo-obstruction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intestinal pseudo-obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
anovulation; infertility, female; polycystic ovary syndrome Gene Set From 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.
breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene Set From 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.
Female Hypogonadism Syndrome Gene Set From 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.
Female Athlete Triad Syndrome Gene Set From 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.
digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Infertility, Female Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Infertility, Female from the curated CTD Gene-Disease Associations dataset.
Genital Neoplasms, Female Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
infertility, female; recurrence Gene Set From 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 Set From 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 Set From 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.
abortion, habitual; infertility, female Gene Set From 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.
colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene Set From 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.
female infertility Gene Set From 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.
chlamydia infections; genital diseases, female Gene Set From 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.
endometriosis; infertility, female Gene Set From 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; infertility, male Gene Set From 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.
abortion, habitual; activated protein c resistance; infertility, female; thrombophilia Gene Set From 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.
postnatal female survival Gene Set From 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.
infertility, female; primary ovarian insufficiency Gene Set From 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 Set From 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 Set From 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.
abortion, habitual; embryo loss; infertility, female Gene Set From 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.
chlamydia infections; infertility, female Gene Set From 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.
genital diseases, female Gene Set From 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 Set From 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 Set From 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.
chlamydia infections; fallopian tube diseases; infertility, female Gene Set From 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.
male-to-female transsexualism Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
female infertility Gene Set From 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.
abnormality of female internal genitalia Gene Set From 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 Set From 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 Set From 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 Set From 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.
Infertility, Female Gene Set From 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.
Genital Neoplasms, Female Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal female reproductive system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
female infertility Gene Set From MPO Gene-Phenotype Associations gene mutations causing the female infertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
reduced female fertility Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From OMIM Gene-Disease Associations genes associated with the luteinizing hormone resistance, female phenotype from the curated OMIM Gene-Disease Associations dataset.
female Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Malignant Female Reproductive System Neoplasm Gene Set From 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 Set From 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 Set From 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.
Female Infertility Associated With Anovulation Gene Set From 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.
Infiltrating Duct Carcinoma Of Female Breast Gene Set From 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 Set From 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 Set From 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 Set From 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.
Abnormality Of Female Internal Genitalia Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Luteinizing Hormone Resistance, Female Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Infertility Gene Set From 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 Sterility Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced female fertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
female infertility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the female infertility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal female meiosis Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 infertility Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the female infertility phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Female steroid hormones in cardiomyocyte energy metabolism Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 infertility of uterine origin Gene Set From 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 breast nipple and areola cancer Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
Female infertility Gene Set From 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 Set From 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.
Facial attractiveness (female raters) Gene Set From 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 Set From 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.
Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Lynch syndrome:Turcot syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marfan's syndrome:Marfan's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome:Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
IFAP syndrome with or without BRESHECK syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome I:Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset.
Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset.
menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cornelia de lange syndrome; de lange syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set From GAD Gene-Disease Associations genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
restless legs syndrome; tourette syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; uveomeningoencephalitic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; uveomeningoencephalitic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melas syndrome; merrf syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease melas syndrome; merrf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From 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.
abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angelman syndrome; rett syndrome; seizures Gene Set From GAD Gene-Disease Associations genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
metabolic syndrome ; metabolic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease metabolic syndrome ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
digeorge syndrome; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene Set From GAD Gene-Disease Associations genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; ehlers-danlos syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; ehlers-danlos syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; felty's syndrome; large granular lymphocyte syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set From GAD Gene-Disease Associations genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart-hand syndrome, holt-oram syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia Gene Set From GAD Gene-Disease Associations genes associated with the disease gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene Set From GAD Gene-Disease Associations genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene Set From GAD Gene-Disease Associations genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
digeorge syndrome/velocardiofacial syndrome complex-2 Gene Set From OMIM Gene-Disease Associations genes associated with the digeorge syndrome/velocardiofacial syndrome complex-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ifap syndrome with or without bresheck syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Miller-Mckusick-Malvaux-Syndrome (3M Syndrome) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Crouzon syndrome-acanthosis nigricans syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Crouzon syndrome-acanthosis nigricans syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Noonan syndrome and Noonan-related syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Crouzon syndrome-acanthosis nigricans syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Crouzon syndrome-acanthosis nigricans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfan Syndrome/Loeys-Dietz Syndrome/Familial Thoracic Aortic Aneurysms and Dissections phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked cerebral-cerebellar-coloboma syndrome syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked cerebral-cerebellar-coloboma syndrome syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
visceral fat deposits and the metabolic syndrome Gene Set From Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.
Branchiootic syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Branchiootic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome, type 3, with hypocalciuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome, type 3, with hypocalciuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple synostoses syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sjögren-Larsson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sjögren-Larsson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hennekam lymphangiectasia-lymphedema syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hennekam lymphangiectasia-lymphedema syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
UV-sensitive syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the UV-sensitive syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib-polydactyly syndrome, Majewski type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Char syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Char syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fragile X syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fragile X syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Shwachman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Shwachman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Greig cephalopolysyndactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Greig cephalopolysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Melnick-Fraser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Melnick-Fraser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marfan's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Melnick-Needles syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Melnick-Needles syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Branchiootorenal syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Branchiootorenal syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly polymicrogyria-polydactyly hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
PTEN hamartoma tumor syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the PTEN hamartoma tumor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lesch-Nyhan syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lesch-Nyhan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oculofaciocardiodental syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oculofaciocardiodental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Robinow Sorauf syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Robinow Sorauf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
17q2131 microdeletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 17q2131 microdeletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Desbuquois syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Desbuquois syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly/autism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly/autism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mohr-Tranebjaerg syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mohr-Tranebjaerg syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 9 (encephalomyopathic with methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osteopenic nonfracture syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteopenic nonfracture syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Barakat syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Barakat syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Raine syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Raine syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Digitorenocerebral syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Digitorenocerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bare Lymphocyte Syndrome, Type II, Complementation Group D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bare Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alport syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alstrom syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alstrom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperinsulinism-hyperammonemia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperinsulinism-hyperammonemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal multiple pterygium syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MORM syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MORM syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Upshaw-Schulman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Upshaw-Schulman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Martsolf syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Martsolf syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome 2q32-q33 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome 2q32-q33 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Blepharophimosis-ptosis-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Blepharophimosis-ptosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Borrone Di Rocco Crovato syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Borrone Di Rocco Crovato syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hurler syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hurler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Angelman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Angelman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lig4 syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lig4 syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 4B, MNGIE type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 4B, MNGIE type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rubinstein-Taybi syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rubinstein-Taybi syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hajdu-Cheney syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hajdu-Cheney syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperferritinemia cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperferritinemia cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Temtamy preaxial brachydactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Temtamy preaxial brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperimmunoglobulin E syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bannayan-Riley-Ruvalcaba syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bannayan-Riley-Ruvalcaba syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chudley-McCullough syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chudley-McCullough syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Poretti-boltshauser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Poretti-boltshauser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bosch-boonstra-schaaf optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frank Ter Haar syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frank Ter Haar syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Androgen resistance syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Androgen resistance syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoparathyroidism retardation dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoparathyroidism retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Holt-Oram syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Holt-Oram syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duane syndrome type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duane syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Young Simpson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Young Simpson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Frasier syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Frasier syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
C-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the C-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meier-Gorlin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meier-Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pili torti-deafness syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pili torti-deafness syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gorlin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gorlin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marshall syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marshall syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carpenter syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carpenter syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bernard-Soulier syndrome, type A2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bernard-Soulier syndrome, type A2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Duane-radial ray syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duane-radial ray syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
22q133 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 22q133 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis laxa-corneal clouding-oligophrenia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis laxa-corneal clouding-oligophrenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TNF receptor-associated periodic fever syndrome (TRAPS) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the TNF receptor-associated periodic fever syndrome (TRAPS) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Waardenburg syndrome type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Waardenburg syndrome type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Steel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Steel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome 1q43-q44 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome 1q43-q44 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Roberts-SC phocomelia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Roberts-SC phocomelia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bloom syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bloom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
McLeod neuroacanthocytosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the McLeod neuroacanthocytosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebrooculofacioskeletal syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebrooculofacioskeletal syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebrooculofacioskeletal syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebrooculofacioskeletal syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nicolaides-Baraitser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nicolaides-Baraitser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nager syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nager syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chédiak-Higashi syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chédiak-Higashi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kindler's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kindler's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carnevale syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carnevale syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kenny syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kenny syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rienhoff syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rienhoff syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Weaver syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Weaver syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia/short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Siderius X-linked mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lymphoproliferative syndrome, ebv-associated, autosomal, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lymphoproliferative syndrome, ebv-associated, autosomal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kohlschutter's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kohlschutter's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked mental retardation with marfanoid habitus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebro-oculo-facio-skeletal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebro-oculo-facio-skeletal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis-lymphedema-telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis-lymphedema-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LEOPARD syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LEOPARD syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Treacher collins syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Treacher collins syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wiskott-Aldrich syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wiskott-Aldrich syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Episodic pain syndrome, familial, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Episodic pain syndrome, familial, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyper-IgE syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyper-IgE syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tourette Syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tourette Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macrocephaly, macrosomia, facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macrocephaly, macrosomia, facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome antenatal type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome antenatal type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome antenatal type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome antenatal type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gamstorp-Wohlfart syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gamstorp-Wohlfart syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Turcot syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sick sinus syndrome 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sick sinus syndrome 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyaline fibromatosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyaline fibromatosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Weill-Marchesani-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Weill-Marchesani-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Netherton syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Netherton syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome, type 4b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome, type 4b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Feingold syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Feingold syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knuckle pads, deafness AND leukonychia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Waardenburg syndrome type 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Waardenburg syndrome type 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Richieri Costa Pereira syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Richieri Costa Pereira syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune lymphoproliferative syndrome, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune lymphoproliferative syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bartter syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bartter syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, fast-channel Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 12 (cardiomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Costello syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Costello syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ochoa syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ochoa syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bruck syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bruck syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bruck syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bruck syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Achalasia-alacrima syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Achalasia-alacrima syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cryptophthalmos syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cryptophthalmos syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nijmegen breakage syndrome-like disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nijmegen breakage syndrome-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brugada syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brugada syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ovarian hyperstimulation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ovarian hyperstimulation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Otofaciocervical syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Otofaciocervical syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kaufman oculocerebrofacial syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kaufman oculocerebrofacial syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome, type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Branchiooculofacial syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Branchiooculofacial syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Karak syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Karak syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Long QT syndrome 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Long QT syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky Pudlak syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky Pudlak syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tarsal carpal coalition syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tarsal carpal coalition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jankovic Rivera syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jankovic Rivera syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nakajo syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nakajo syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chromosome Xq28 deletion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chromosome Xq28 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fanconi-Bickel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fanconi-Bickel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
short QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the short QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Smith-Lemli-Opitz syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Smith-Lemli-Opitz syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Von Hippel-Lindau syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Usher syndrome, type 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Usher syndrome, type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome progeroid type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome progeroid type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Larsen syndrome, dominant type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Larsen syndrome, dominant type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, musculocontractural type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, musculocontractural type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Temtamy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Temtamy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Birk Barel mental retardation dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Birk Barel mental retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alport syndrome, X-linked recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alport syndrome, X-linked recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperphosphatasia with mental retardation syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adenomatous polyposis coli:Gardner syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adenomatous polyposis coli:Gardner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leprechaunism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leprechaunism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Simpson-Golabi-Behmel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Simpson-Golabi-Behmel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Robinow syndrome, autosomal recessive, with brachy-syn-polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
XFE progeroid syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the XFE progeroid syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leigh syndrome due to mitochondrial complex I deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dysequilibrium syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dysequilibrium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atypical hemolytic-uremic syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atypical hemolytic-uremic syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atypical hemolytic-uremic syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atypical hemolytic-uremic syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Johanson-Blizzard syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Johanson-Blizzard syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
GRACILE syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the GRACILE syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked lymphoproliferative syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked lymphoproliferative syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kowarski syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kowarski syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ADULT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ADULT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel-Gruber syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel-Gruber syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked lymphoproliferative syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked lymphoproliferative syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neutrophil immunodeficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neutrophil immunodeficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coffin-Lowry syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coffin-Lowry syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auriculocondylar syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auriculocondylar syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auriculocondylar syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auriculocondylar syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, hydroxylysine-deficient Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, hydroxylysine-deficient phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pierson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pierson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pfeiffer syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pfeiffer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Loeys-Dietz syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tricho-dento-osseous syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tricho-dento-osseous syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mowat-Wilson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mowat-Wilson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Perrault syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Perrault syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jensen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jensen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Werner syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Werner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aarskog syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aarskog syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Enamel-renal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Enamel-renal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 21 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 22 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple synostoses syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple synostoses syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Popliteal pterygium syndrome lethal type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Popliteal pterygium syndrome lethal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Keutel syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Keutel syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pitt-Hopkins syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Segawa syndrome, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Segawa syndrome, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple pterygium syndrome Escobar type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pitt-Hopkins-like syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins-like syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pitt-Hopkins-like syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pitt-Hopkins-like syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lynch syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital short bowel syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
C syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the C syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Klippel-Feil syndrome 2, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Klippel-Feil syndrome 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stiff skin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stiff skin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lenz microphthalmia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lenz microphthalmia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive hypohidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marshall/Stickler syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marshall/Stickler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schwartz Jampel syndrome type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schwartz Jampel syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Grebe syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Grebe syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Saethre-Chotzen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Saethre-Chotzen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, slow-channel congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Floating-Harbor syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Floating-Harbor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warburg micro syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warburg micro syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warburg micro syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warburg micro syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hermansky-Pudlak syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hermansky-Pudlak syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Osler hemorrhagic telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osler hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wieacker syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wieacker syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kabuki make-up syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kabuki make-up syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cohen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cohen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oligodontia-colorectal cancer syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oligodontia-colorectal cancer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Filippi syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Filippi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contractural syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primrose syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primrose syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Perrault syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Perrault syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marshall-Smith syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marshall-Smith syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Loeys-Dietz syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brittle cornea syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brittle cornea syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rotor syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rotor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oral-facial-digital syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oral-facial-digital syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acrocallosal syndrome, Schinzel type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acrocallosal syndrome, Schinzel type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gray platelet syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gray platelet syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mast syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mast syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Amish infantile epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Amish infantile epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meacham syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meacham syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stormorken syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stormorken syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Opitz-Frias syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Opitz-Frias syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardio-facio-cutaneous syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardio-facio-cutaneous syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Yunis Varon syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Yunis Varon syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cowden syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cowden syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mulibrey nanism syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mulibrey nanism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ohdo syndrome, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ohdo syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, idiopathic, steroid-resistant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, idiopathic, steroid-resistant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Townes-Brocks-branchiootorenal-like syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Townes-Brocks-branchiootorenal-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
SeSAME syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the SeSAME syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Odontotrichomelic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Odontotrichomelic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome, type 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile liver failure syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile liver failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lowe syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lowe syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, type 7B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, musculocontractural type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, musculocontractural type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett syndrome, congenital variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Van Maldergem syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Van Maldergem syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Robinow syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Robinow syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bone marrow failure syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bone marrow failure syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Orofaciodigital syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Orofaciodigital syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Orofaciodigital syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Orofaciodigital syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distichiasis-lymphedema syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distichiasis-lymphedema syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Townes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Townes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neu-Laxova syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neu-Laxova syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Winchester syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Winchester syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Unverricht-Lundborg syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Unverricht-Lundborg syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Verheij syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Verheij syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rapp-Hodgkin ectodermal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rapp-Hodgkin ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Allan-Herndon-Dudley syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Allan-Herndon-Dudley syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sick sinus syndrome 1, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sick sinus syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arterial tortuosity syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arterial tortuosity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Papillon-Lefèvre syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Papillon-Lefèvre syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Brown-vialetto-van laere syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Brown-vialetto-van laere syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, epilepsy, and diabetes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peters plus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peters plus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ulnar-mammary syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ulnar-mammary syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Insulin-dependent diabetes mellitus secretory diarrhea syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Insulin-dependent diabetes mellitus secretory diarrhea syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Zunich neuroectodermal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Beckwith-Wiedemann syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Beckwith-Wiedemann syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Van Maldergem Wetzburger Verloes syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Van Maldergem Wetzburger Verloes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sotos' syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sotos' syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dyggve-Melchior-Clausen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dyggve-Melchior-Clausen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Baraitser-Winter Syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Baraitser-Winter Syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Three M syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Three M syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Howel-Evans syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Howel-Evans syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Senior-Loken syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Senior-Loken syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Senior-Loken syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Senior-Loken syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rhabdoid tumor predisposition syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rhabdoid tumor predisposition syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tatton-Brown-rahman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tatton-Brown-rahman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
COACH syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the COACH syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib polydactyly syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short rib polydactyly syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short rib polydactyly syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Enhanced s-cone syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Enhanced s-cone syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked hydrocephalus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked hydrocephalus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Acquired long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Acquired long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Van der Woude syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Van der Woude syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cornelia de Lange syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cornelia de Lange syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sudden infant death syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sudden infant death syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dursun syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dursun syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carpenter syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carpenter syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Li-Fraumeni syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Li-Fraumeni syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Haim-Munk syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Haim-Munk syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Knobloch syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Knobloch syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Carbohydrate-deficient glycoprotein syndrome type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Carbohydrate-deficient glycoprotein syndrome type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Advanced sleep phase syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Advanced sleep phase syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoplastic enamel-onycholysis-hypohidrosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoplastic enamel-onycholysis-hypohidrosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jarcho-Levin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jarcho-Levin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cornelia de Lange syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cornelia de Lange syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cornelia de Lange syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cornelia de Lange syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cornelia de Lange syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cornelia de Lange syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal recessive Dejerine-Sottas syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal recessive Dejerine-Sottas syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kabuki syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kabuki syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hay-Wells syndrome of ectodermal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hay-Wells syndrome of ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 13 (encephalomyopathic type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Reynolds syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Reynolds syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glut1 deficiency syndrome 1, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glut1 deficiency syndrome 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 12/15, digenic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 12/15, digenic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Serkal syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Serkal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Marinesco-Sjögren syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Marinesco-Sjögren syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Seckel syndrome 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Seckel syndrome 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Seckel syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Seckel syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Seckel syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Seckel syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Seckel syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Seckel syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neu-laxova syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neu-laxova syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Urofacial syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Urofacial syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gordon's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gordon's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arts syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arts syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
McKusick Kaufman syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the McKusick Kaufman syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune polyglandular syndrome type 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune polyglandular syndrome type 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rubinstein-Taybi syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rubinstein-Taybi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
FG syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the FG syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Loeys-Dietz syndrome, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyglandular autoimmune syndrome, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyglandular autoimmune syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bernard-Soulier syndrome, type A1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bernard-Soulier syndrome, type A1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis renal dysfunction cholestasis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis renal dysfunction cholestasis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
EEM syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the EEM syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiofaciocutaneous syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiofaciocutaneous syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
TARP syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the TARP syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the AUTOIMMUNE POLYENDOCRINOPATHY SYNDROME, TYPE I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Drash syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Drash syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, hiatal hernia and nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pallister-Hall syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pallister-Hall syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Radial aplasia-thrombocytopenia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Radial aplasia-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Griscelli syndrome type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Griscelli syndrome type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Griscelli syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Griscelli syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Caudal regression syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Caudal regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Catel Manzke syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Catel Manzke syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trichohepatoenteric syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trichohepatoenteric syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cockayne syndrome type A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cockayne syndrome type A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Warsaw breakage syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Warsaw breakage syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Popliteal pterygium syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Popliteal pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
SHORT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the SHORT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Jervell and Lange-Nielsen syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bainbridge-Ropers syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bainbridge-Ropers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Orofaciodigital syndrome xiv Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Orofaciodigital syndrome xiv phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leigh syndrome, French Canadian type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome, French Canadian type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME Gene Set From ClinVar Gene-Phenotype Associations genes associated with the XERODERMA PIGMENTOSUM, TYPE F/COCKAYNE SYNDROME phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bent bone dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bent bone dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pachydermoperiostosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pachydermoperiostosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bardet-Biedl syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bardet-Biedl syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Crouzon syndrome with acanthosis nigricans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Crouzon syndrome with acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leigh syndrome due to mitochondrial complex II deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nance-Horan syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nance-Horan syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple mitochondrial dysfunctions syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple mitochondrial dysfunctions syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Saethre-Chotzen syndrome with eyelid anomalies Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Saethre-Chotzen syndrome with eyelid anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gerstmann-Straussler-Scheinker syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gerstmann-Straussler-Scheinker syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Curry-Hall syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Curry-Hall syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial multiple polyposis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kartagener syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kartagener syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutis Gyrata syndrome of Beare and Stevenson Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Donnai Barrow syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Donnai Barrow syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Klippel-Feil syndrome 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Klippel-Feil syndrome 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dubin-Johnson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dubin-Johnson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Loeys-Dietz syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Riddle syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Riddle syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cold-induced sweating syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cold-induced sweating syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Oto-palato-digital syndrome, type I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Oto-palato-digital syndrome, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cockayne syndrome, type B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cockayne syndrome, type B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Wagner syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Wagner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR Gene Set From ClinVar Gene-Phenotype Associations genes associated with the STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Schinzel-Giedion syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Schinzel-Giedion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bowen-Conradi syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bowen-Conradi syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
ATR-X syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the ATR-X syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gardner syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gardner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Baller-Gerold syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Baller-Gerold syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypocalcemia, autosomal dominant 1, with bartter syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypocalcemia, autosomal dominant 1, with bartter syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylocarpotarsal synostosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylocarpotarsal synostosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
LONG QT SYNDROME 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the LONG QT SYNDROME 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal coloboma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal coloboma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Menkes kinky-hair syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Menkes kinky-hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Legius syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Legius syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Andermann syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Andermann syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Michels syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Michels syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stocco dos Santos syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stocco dos Santos syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sotos syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sotos syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lenz-Majewski hyperostosis syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lenz-Majewski hyperostosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Axenfeld-Rieger syndrome type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Axenfeld-Rieger syndrome type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Axenfeld-Rieger syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Axenfeld-Rieger syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lethal congenital contracture syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitchell-Riley syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitchell-Riley syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tietz syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tietz syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Prune belly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Prune belly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alagille syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alagille syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alagille syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alagille syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mosaic variegated aneuploidy syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mosaic variegated aneuploidy syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Christianson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Christianson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Histiocytosis-lymphadenopathy plus syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Histiocytosis-lymphadenopathy plus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin fragility woolly hair syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin fragility woolly hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Loeys-Dietz syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Loeys-Dietz syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cortical dysplasia-focal epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spondylocheirodysplasia, Ehlers-Danlos syndrome-like Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spondylocheirodysplasia, Ehlers-Danlos syndrome-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital long QT syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Three M syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Three M syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Symphalangism-brachydactyly syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Symphalangism-brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rhabdoid tumor predisposition syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rhabdoid tumor predisposition syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Treacher collins syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Treacher collins syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stickler syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stickler syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Trichorhinophalangeal syndrome type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trichorhinophalangeal syndrome type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Enlarged vestibular aqueduct syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Enlarged vestibular aqueduct syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Temple-Baraitser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Temple-Baraitser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Boucher Neuhauser syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Boucher Neuhauser syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stuve-Wiedemann syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stuve-Wiedemann syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyendocrine-polyneuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyendocrine-polyneuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adams-Oliver syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adams-Oliver syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adams-Oliver syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adams-Oliver syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adams-Oliver syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adams-Oliver syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adams-Oliver syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adams-Oliver syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autoimmune lymphoproliferative syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autoimmune lymphoproliferative syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucose transporter type 1 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Perry syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Perry syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Freeman-Sheldon syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Freeman-Sheldon syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adams-Oliver syndrome 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adams-Oliver syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ehlers-Danlos syndrome, type 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos syndrome, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alacrima, achalasia, and mental retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly-capillary malformation syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly-capillary malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Roussy-Lévy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Roussy-Lévy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
atypical hemolytic-uremic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the atypical hemolytic-uremic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA-depletion syndrome 3, hepatocerebral Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA-depletion syndrome 3, hepatocerebral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nephrotic syndrome, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nephrotic syndrome, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renpenning syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renpenning syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pendred's syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pendred's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
FG syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the FG syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cocoon syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cocoon syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hennekam lymphangiectasia-lymphedema syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hennekam lymphangiectasia-lymphedema syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Kallmann syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallmann syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bare lymphocyte syndrome type 2, complementation group E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bare lymphocyte syndrome type 2, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bare lymphocyte syndrome type 2, complementation group A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bare lymphocyte syndrome type 2, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Borjeson-Forssman-Lehmann syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Borjeson-Forssman-Lehmann syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rothmund-Thomson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rothmund-Thomson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Meckel syndrome, type 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Meckel syndrome, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Activated PI3K-delta syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Activated PI3K-delta syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Snyder Robinson syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Snyder Robinson syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Weill-Marchesani syndrome 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Weill-Marchesani syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Reifenstein syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Reifenstein syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rapadilino syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rapadilino syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tumor predisposition syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Tumor predisposition syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Joubert syndrome 9/15, digenic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Joubert syndrome 9/15, digenic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Immunodeficiency-centromeric instability-facial anomalies syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency-centromeric instability-facial anomalies syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mitochondrial DNA depletion syndrome 7 (hepatocerebral type) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Scalp ear nipple syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Scalp ear nipple syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Majeed syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Majeed syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cutaneous telangiectasia and cancer syndrome, familial Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aicardi-goutieres syndrome 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aicardi-goutieres syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aicardi-goutieres syndrome 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aicardi-goutieres syndrome 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dejerine-Sottas syndrome, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dejerine-Sottas syndrome, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

Female Pseudo-Turner Syndrome Gene Set

chlamydia infections; genital diseases, female; infertility, female; inflammation Gene Set

pseudo-torch syndrome Gene Set

Pseudo-Torch Syndrome Gene Set

Pseudo-Bartter Syndrome Gene Set

Pseudo-Zellweger Syndrome Gene Set

pseudo-TORCH syndrome 1 Gene Set

Neonatal pseudo-hydrocephalic progeroid syndrome Gene Set

Pseudo-TORCH syndrome Gene Set

endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

Pseudo von Willebrand disease Gene Set

Pseudo-Hurler polydystrophy Gene Set

intestinal pseudo-obstruction Gene Set

colonic pseudo-obstruction Gene Set

intestinal pseudo-obstruction Gene Set

intestinal pseudo-obstruction; mitochondrial diseases Gene Set

deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence Gene Set

pseudo Gene Set

intestinal pseudo-obstruction Gene Set

Intestinal Pseudo-Obstruction Gene Set

Smaug, pseudo-HEAT analogous topology Gene Set

Chronic Intestinal Pseudo-Obstruction Gene Set

Intestinal Pseudo-Obstruction Gene Set

Pseudo-Fractures Gene Set

Pseudo-Hurler Polydystrophy Gene Set

Pseudo Pelger-Huet Anomaly Gene Set

Intestinal pseudo-obstruction Gene Set

Intestinal pseudo-obstruction Gene Set

Colonic pseudo-obstruction Gene Set

X-linked chronic idiopathic intestinal pseudo-obstruction Gene Set

Pseudo-Hurler polydystrophy Gene Set

Pseudo von Willebrand disease Gene Set

Intestinal pseudo-obstruction Gene Set

anovulation; infertility, female; polycystic ovary syndrome Gene Set

breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene Set

Female Hypogonadism Syndrome Gene Set

Female Athlete Triad Syndrome Gene Set

digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set

Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene Set

female germ cell nucleus Gene Set

female pronucleus Gene Set

female germline ring canal Gene Set

female germline ring canal inner rim Gene Set

female germ cell nucleus Gene Set

female pronucleus Gene Set

Infertility, Female Gene Set

Genital Neoplasms, Female Gene Set

Epilepsy, Female-Restricted, with Mental Retardation Gene Set

Female Urogenital Diseases Gene Set

Genital Diseases, Female Gene Set

female reproductive system disease Gene Set

female reproductive organ cancer Gene Set

female reproductive organ benign neoplasm Gene Set

female reproductive system disease Gene Set

female urethral cancer Gene Set

female breast cancer Gene Set

female stress incontinence Gene Set

female reproductive system disease Gene Set

female reproductive organ cancer Gene Set

female breast carcinoma Gene Set

female reproductive organ benign neoplasm Gene Set

prolapse of female genital organ Gene Set

female reproductive endometrioid cancer Gene Set

female preferences for male odors Gene Set

infertility, female; recurrence Gene Set

infertility, female; pof - premature ovarian failure; primary ovarian insufficiency Gene Set

infertility, female; ovarian failure, premature Gene Set

abortion, habitual; infertility, female Gene Set

colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene Set

female infertility Gene Set

chlamydia infections; genital diseases, female Gene Set

endometriosis; infertility, female Gene Set

infertility, female; infertility, male Gene Set

abortion, habitual; activated protein c resistance; infertility, female; thrombophilia Gene Set

postnatal female survival Gene Set

infertility, female; primary ovarian insufficiency Gene Set

endometriosis; infertility, female; ovarian cyst, nos; ovarian cysts Gene Set

infertility, female Gene Set