Name

polycystic ovaries and premature male pattern baldness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovaries and premature male pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

male-pattern baldness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease male-pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

male pattern baldness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease male pattern baldness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Male-pattern baldness Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Male-pattern baldness phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes; obstetric labor, premature; pre-eclampsia; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovaries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the polycystic ovaries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

polycystic ovaries Gene Set

From HPO Gene-Disease Associations

genes associated with the polycystic ovaries phenotype by mapping known disease genes to disease phenotypes from the HPO 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

ovaries Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ovaries in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

baldness Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term baldness in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

LHX8_Deficiency_GDS3254_600_mouse_Newborn ovaries Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the LHX8_Deficiency_GDS3254_600_mouse_Newborn ovaries gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

polycystic ovary syndrome; premature ovarian failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome; premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal membranes, premature rupture; premature birth; uterine prolapse Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal membranes, premature rupture; premature birth; uterine prolapse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal membranes, premature rupture; obstetric labor, premature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal membranes, premature rupture; obstetric labor, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amenorrhea; ovarian failure, premature; pof - premature ovarian failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amenorrhea; ovarian failure, premature; pof - premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial vaginosis; fetal membranes, premature rupture; obstetric labor, premature; pregnancy complications, infectious; vaginosis, bacterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial vaginosis; fetal membranes, premature rupture; obstetric labor, premature; pregnancy complications, infectious; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal membranes, premature rupture; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal membranes, premature rupture; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ovarian failure, premature; pof - premature ovarian failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ovarian failure, premature; pof - premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature birth following premature rupture of fetal membranes Gene Set

From HPO Gene-Disease Associations

genes associated with the premature birth following premature rupture of fetal membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

polycystic kidney and hepatic disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney and hepatic disease phenotype from the curated OMIM Gene-Disease Associations dataset.

chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; fetal membranes, premature rupture; infection of amniotic sac and membranes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature coronary artery disease and familial hypoalphalipoproteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature coronary artery disease and familial hypoalphalipoproteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; infection of amniotic sac and membranes; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; infection of amniotic sac and membranes; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Deafness, Sensorineural, And Male Infertility Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Sensorineural, And Male Infertility from the curated CTD Gene-Disease Associations dataset.

wilms' tumor and congenital male genitourinary malformation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease wilms' tumor and congenital male genitourinary malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced trans-activation impaired sperm production and male infertility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced trans-activation impaired sperm production and male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness and male infertility Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness and male infertility phenotype from the curated OMIM Gene-Disease Associations dataset.

pattern Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term pattern in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

embryonic heart tube anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

proximal/distal pattern formation involved in nephron development Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations dataset.

regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

anterior compartment pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the anterior compartment pattern formation biological process from the curated GO Biological Process Annotations dataset.

cytoplasmic pattern recognition receptor signaling pathway in response to virus Gene Set

From GO Biological Process Annotations

genes participating in the cytoplasmic pattern recognition receptor signaling pathway in response to virus biological process from the curated GO Biological Process Annotations dataset.

pattern specification involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

proximal/distal pattern formation involved in metanephric nephron development Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

lung pattern specification process Gene Set

From GO Biological Process Annotations

genes participating in the lung pattern specification process biological process from the curated GO Biological Process Annotations dataset.

neural plate pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the neural plate pattern specification biological process from the curated GO Biological Process Annotations dataset.

cell fate commitment involved in pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the cell fate commitment involved in pattern specification biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

compartment pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the compartment pattern specification biological process from the curated GO Biological Process Annotations dataset.

cell fate specification involved in pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the cell fate specification involved in pattern specification biological process from the curated GO Biological Process Annotations dataset.

pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

embryonic pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the embryonic pattern specification biological process from the curated GO Biological Process Annotations dataset.

regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

pattern specification involved in metanephros development Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification involved in metanephros development biological process from the curated GO Biological Process Annotations dataset.

forebrain dorsal/ventral pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the forebrain dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations dataset.

radial pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the radial pattern formation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

dorsal/ventral pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the dorsal/ventral pattern formation biological process from the curated GO Biological Process Annotations dataset.

pattern specification involved in mesonephros development Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification involved in mesonephros development biological process from the curated GO Biological Process Annotations dataset.

fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

left/right pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the left/right pattern formation biological process from the curated GO Biological Process Annotations dataset.

cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

cell surface pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the cell surface pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

pattern specification process Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification process biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in ureteric bud development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in ureteric bud development biological process from the curated GO Biological Process Annotations dataset.

regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

forebrain anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the forebrain anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube left/right pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube left/right pattern formation biological process from the curated GO Biological Process Annotations dataset.

pattern specification involved in pronephros development Gene Set

From GO Biological Process Annotations

genes participating in the pattern specification involved in pronephros development biological process from the curated GO Biological Process Annotations dataset.

proximal/distal pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations dataset.

cell fate determination involved in pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the cell fate determination involved in pattern specification biological process from the curated GO Biological Process Annotations dataset.

signaling pattern recognition receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the signaling pattern recognition receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

pattern binding Gene Set

From GO Molecular Function Annotations

genes performing the pattern binding molecular function from the curated GO Molecular Function Annotations dataset.

pattern recognition receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the pattern recognition receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

termporal pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the termporal pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

acquired abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

reduced amplitude of pattern visual evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced amplitude of pattern visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal branching pattern of the aortic arch Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

termporal pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the termporal pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pattern of respiration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

acquired abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Pattern Recognition, Physiological Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Pattern Recognition, Physiological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Pattern Recognition, Visual Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Pattern Recognition, Visual phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

abnormal sympathetic neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mammary gland pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mammary gland pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal non-rapid eye movement sleep pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal non-rapid eye movement sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urination pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urination pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain wave pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain wave pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal central pattern generator function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal central pattern generator function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal breathing pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal breathing pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear ihc efferent innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear ihc efferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sensory neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sensory neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sleep pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal paradoxical sleep pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal paradoxical sleep pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear ihc afferent innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear ihc afferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal innervation pattern to muscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal innervation pattern to muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal olfactory neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal olfactory neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal phrenic nerve innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal phrenic nerve innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal blood vessel pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear ohc efferent innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear ohc efferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal enamel rod pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal enamel rod pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal motor neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal motor neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal phrenic nerve innervation pattern to diaphragm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal phrenic nerve innervation pattern to diaphragm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

distorted hair follicle pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the distorted hair follicle pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear ohc afferent innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear ohc afferent innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.

Polycystic kidney disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, adult type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, adult type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic kidney disease, infantile type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polycystic kidney disease, infantile type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polycystic liver disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic liver disease from the curated CTD Gene-Disease Associations dataset.

Polycystic Kidney, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic Kidney, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Polycystic Kidney, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic Kidney, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Polycystic Ovary Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic Ovary Syndrome from the curated CTD Gene-Disease Associations dataset.

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy from the curated CTD Gene-Disease Associations dataset.

Polycystic Kidney Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic Kidney Diseases from the curated CTD Gene-Disease Associations dataset.

Polycystic kidneys, severe infantile with tuberous sclerosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic kidneys, severe infantile with tuberous sclerosis from the curated CTD Gene-Disease Associations dataset.

Polycystic Ovary Syndrome Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Polycystic Ovary Syndrome in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

polycystic kidney disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease polycystic kidney disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

polycystic ovary syndrome Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease polycystic ovary syndrome in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

polycystic kidney disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease polycystic kidney disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

polycystic liver disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease polycystic liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

polycystic ovary syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease polycystic ovary syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

polycystic ovary syndrome; hyperandrogenism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome; hyperandrogenism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nephritis, interstitial; polycystic kidney diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nephritis, interstitial; polycystic kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic kidney disease 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic kidney disease 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose intolerance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; hyperinsulinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; hyperinsulinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glomerulonephritis, iga; iga glomerulonephritides; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glomerulonephritis, iga; iga glomerulonephritides; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetic nephropathy; polycystic kidney disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetic nephropathy; polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations 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.

polycystic ovary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; hypertension; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acne vulgaris; hirsutism; hyperandrogenism; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acne vulgaris; hirsutism; hyperandrogenism; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovary syndrome; adrenal androgen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome; adrenal androgen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovary syndrome; pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset of esrf in pkd1 adult polycystic kidney disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of esrf in pkd1 adult polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular risk; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular risk; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic kidney disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic kidney disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; glomerulonephritis; kidney failure, chronic; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; insulin resistance; obesity; polycystic ovary syndrome; leanness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovary syndrome; leanness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovary syndrome; diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome; diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic liver disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; polycystic ovarian syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; polycystic ovarian syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amenorrhea; hirsutism; insulin resistance; obesity; oligomenorrhea; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amenorrhea; hirsutism; insulin resistance; obesity; oligomenorrhea; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic kidney diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; glucose; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; glucose; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glomerulonephritis, iga; kidney failure, chronic; polycystic kidney diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glomerulonephritis, iga; kidney failure, chronic; polycystic kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; polycystic ovary syndrome; androgen levels; anthropometric measuments Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; polycystic ovary syndrome; androgen levels; anthropometric measuments in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovary syndrome (pcos) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome (pcos) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; polycystic ovary syndrome; hormone disturbance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; polycystic ovary syndrome; hormone disturbance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; polycystic ovarian syndrome; hyperandrogenism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; polycystic ovarian syndrome; hyperandrogenism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; polycystic ovary syndrome 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.

polycystic kidney, autosomal dominant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic kidney, autosomal dominant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovary syndrome; testosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; insulin resistance; overweight; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; insulin resistance; overweight; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; polycystic ovary syndrome; hormone disturbance; sex hormones Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; polycystic ovary syndrome; hormone disturbance; sex hormones in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovary syndrome. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovary syndrome. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term polycystic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Polycystic Ovary Syndrome_Skeletal muscle_GSE6798 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Polycystic Ovary Syndrome_Skeletal muscle_GSE6798 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Polycystic Ovary Syndrome_Adipose tissue_GSE5090 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Polycystic Ovary Syndrome_Adipose tissue_GSE5090 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Polycystic ovary syndrome Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Polycystic ovary syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

polycystic ovary syndrome Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease polycystic ovary syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

polycystic liver disease Gene Set

From HPO Gene-Disease Associations

genes associated with the polycystic liver disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

polycystic kidney dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the polycystic kidney dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Polycystic Kidney, Autosomal Dominant Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Polycystic Kidney, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Polycystic Ovary Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Polycystic Ovary Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Polycystic Kidney, Autosomal Recessive Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Polycystic Kidney, Autosomal Recessive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Polycystic Kidney Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Polycystic Kidney Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Polycystic kidney disease type 2 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Polycystic kidney disease type 2 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Polycystic kidney disease type 1 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Polycystic kidney disease type 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

polycystic kidney Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the polycystic kidney phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

polycystic kidney disease 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney disease 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

polycystic kidney disease, adult type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney disease, adult type i phenotype from the curated OMIM Gene-Disease Associations dataset.

polycystic liver disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic liver disease phenotype from the curated OMIM Gene-Disease Associations dataset.

polycystic kidney disease, infantile severe, with tuberous sclerosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney disease, infantile severe, with tuberous sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset.

polycystic ovary syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic ovary syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Premature coronary artery disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature coronary artery disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature ovarian failure 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature ovarian failure 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature ovarian failure 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature ovarian failure 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature ovarian failure 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature ovarian failure 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature ovarian failure 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature ovarian failure 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature ovarian failure 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature ovarian failure 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature ovarian failure 2b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature ovarian failure 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Premature ovarian failure 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Premature ovarian failure 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular Premature Complexes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Premature Complexes from the curated CTD Gene-Disease Associations dataset.

Infant, Premature, Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Infant, Premature, Diseases from the curated CTD Gene-Disease Associations dataset.

Premature Birth Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Premature Birth from the curated CTD Gene-Disease Associations dataset.

Premature Ovarian Failure 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Premature Ovarian Failure 3 from the curated CTD Gene-Disease Associations dataset.

Premature Ovarian Failure 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Premature Ovarian Failure 5 from the curated CTD Gene-Disease Associations dataset.

Premature Ovarian Failure 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Premature Ovarian Failure 7 from the curated CTD Gene-Disease Associations dataset.

Obstetric Labor, Premature Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Obstetric Labor, Premature from the curated CTD Gene-Disease Associations dataset.

Premature Ovarian Failure 2b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Premature Ovarian Failure 2b from the curated CTD Gene-Disease Associations dataset.

Premature Ovarian Failure 2a Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Premature Ovarian Failure 2a from the curated CTD Gene-Disease Associations dataset.

Premature Ovarian Failure 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Premature Ovarian Failure 6 from the curated CTD Gene-Disease Associations dataset.

PREMATURE CHROMATID SEPARATION TRAIT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PREMATURE CHROMATID SEPARATION TRAIT from the curated CTD Gene-Disease Associations dataset.

Aging, Premature Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aging, Premature from the curated CTD Gene-Disease Associations dataset.

Preterm Premature Rupture of the Membranes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Preterm Premature Rupture of the Membranes from the curated CTD Gene-Disease Associations dataset.

premature ovarian failure Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease premature ovarian failure from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

premature ovarian failure Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease premature ovarian failure in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

premature ovarian failure Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease premature ovarian failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

premature menopause Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease premature menopause in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

premature ejaculation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease premature ejaculation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

liver transplant; prostate cancer; premature ovarian failure; lupus nephritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease liver transplant; prostate cancer; premature ovarian failure; lupus nephritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

idiopathic premature ovarian failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease idiopathic premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal membranes, premature rupture; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal membranes, premature rupture; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature birth; vaginosis, bacterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature birth; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; inflammation; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; inflammation; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature ovarian failure; lupus nephritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature ovarian failure; lupus nephritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; premature pubarche Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; premature pubarche in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; pregnancy complications, cardiovascular; premature birth; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; pregnancy complications, cardiovascular; premature birth; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature birth; uterine cervical incompetence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature birth; uterine cervical incompetence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; infant, newborn, diseases; infection; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; infant, newborn, diseases; infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ovarian failure, premature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ovarian failure, premature 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.

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.

brugada syndrome; ventricular fibrillation; ventricular premature complexes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; ventricular fibrillation; ventricular premature complexes 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.

infant, premature, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infant, premature, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal death; pre-eclampsia; pregnancy complications; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal death; pre-eclampsia; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholestasis, intrahepatic; infant, premature, diseases; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholestasis, intrahepatic; infant, premature, diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial premature myocardial infarction. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial premature myocardial infarction. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; inflammation; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; inflammation; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diseases in twins; obstetric labor, premature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diseases in twins; obstetric labor, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; menopause, premature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; menopause, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; placenta diseases; premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhage; placenta diseases; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; infant, premature, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; infant, premature, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pof - premature ovarian failure; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial vaginosis; premature birth; vaginosis, bacterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial vaginosis; premature birth; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blepharophimosis; blepharoptosis; pof - premature ovarian failure; primary ovarian insufficiency; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blepharophimosis; blepharoptosis; pof - premature ovarian failure; primary ovarian insufficiency; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature ovarian failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature ovarian failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications, hematologic; premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications, hematologic; premature birth; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x syndrome; ovarian failure, premature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x syndrome; ovarian failure, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; ventricular premature complexes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; ventricular premature complexes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dental plaque; periodontitis; pregnancy complications; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental plaque; periodontitis; pregnancy complications; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature coronary artery disease. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature coronary artery disease. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal membranes, premature rupture Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal membranes, premature rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obstetric labor, premature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obstetric labor, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature myocardial infarction in men. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature myocardial infarction in men. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ductus arteriosus, patent; patent ductus arteriosus; premature birth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ductus arteriosus, patent; patent ductus arteriosus; premature birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature coronary heart disease. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature coronary heart disease. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infant, premature, diseases; intracranial hemorrhages Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infant, premature, diseases; intracranial hemorrhages in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menopause, premature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menopause, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amenorrhea; pof - premature ovarian failure; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amenorrhea; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

46, xx disorders of sex development; pof - premature ovarian failure; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease 46, xx disorders of sex development; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic retinopathy; obstetric labor, premature; pre-eclampsia; pregnancy in diabetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic retinopathy; obstetric labor, premature; pre-eclampsia; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menopause, premature; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menopause, premature; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bacterial vaginosis; fetal membranes, premature rupture; vaginosis, bacterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bacterial vaginosis; fetal membranes, premature rupture; vaginosis, bacterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature rupture of membranes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature rupture of membranes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypothyroidism; pof - premature ovarian failure; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypothyroidism; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature ovarian failure; primary amenorrhea; secondary amenorrhea Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature ovarian failure; primary amenorrhea; secondary amenorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature ovarian failure; menopause, early Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature ovarian failure; menopause, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; infant, premature, diseases; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; infant, premature, diseases; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature ejaculation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease premature ejaculation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

premature Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term premature in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Premature aging_Skin fibroblast_GSE10123 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Premature aging_Skin fibroblast_GSE10123 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

stress-induced premature senescence Gene Set

From GO Biological Process Annotations

genes participating in the stress-induced premature senescence biological process from the curated GO Biological Process Annotations dataset.

oxidative stress-induced premature senescence Gene Set

From GO Biological Process Annotations

genes participating in the oxidative stress-induced premature senescence biological process from the curated GO Biological Process Annotations dataset.

premature ovarian failure Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease premature ovarian failure in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

premature eruption of permanent teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the premature eruption of permanent teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

premature ovarian failure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the premature ovarian failure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

premature peripheral vascular disease Gene Set

From HPO Gene-Disease Associations

genes associated with the premature peripheral vascular disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature calcification of mitral annulus Gene Set

From HPO Gene-Disease Associations

genes associated with the premature calcification of mitral annulus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature osteoarthritis Gene Set

From HPO Gene-Disease Associations

genes associated with the premature osteoarthritis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased rate of premature chromosome condensation Gene Set

From HPO Gene-Disease Associations

genes associated with the increased rate of premature chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature thelarche Gene Set

From HPO Gene-Disease Associations

genes associated with the premature thelarche phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature graying of hair Gene Set

From HPO Gene-Disease Associations

genes associated with the premature graying of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature birth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature rupture of membranes Gene Set

From HPO Gene-Disease Associations

genes associated with the premature rupture of membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature closure of fontanelles Gene Set

From HPO Gene-Disease Associations

genes associated with the premature closure of fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature fusion of phalangeal epiphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the premature fusion of phalangeal epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature skin wrinkling Gene Set

From HPO Gene-Disease Associations

genes associated with the premature skin wrinkling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature separation of centromeric heterochromatin Gene Set

From HPO Gene-Disease Associations

genes associated with the premature separation of centromeric heterochromatin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of permanent teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of primary teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature ovarian failure Gene Set

From HPO Gene-Disease Associations

genes associated with the premature ovarian failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature arteriosclerosis Gene Set

From HPO Gene-Disease Associations

genes associated with the premature arteriosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature pubarche Gene Set

From HPO Gene-Disease Associations

genes associated with the premature pubarche phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature chromatid separation Gene Set

From HPO Gene-Disease Associations

genes associated with the premature chromatid separation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature delivery because of cervical insufficiency or membrane fragility Gene Set

From HPO Gene-Disease Associations

genes associated with the premature delivery because of cervical insufficiency or membrane fragility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature occlusive vascular disease Gene Set

From HPO Gene-Disease Associations

genes associated with the premature occlusive vascular disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature coronary artery disease Gene Set

From HPO Gene-Disease Associations

genes associated with the premature coronary artery disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Ventricular Premature Complexes Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Premature Complexes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Infant, Premature, Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infant, Premature, Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Premature Birth Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Premature Birth phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Aging, Premature Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Aging, Premature phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Obstetric Labor, Premature Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Obstetric Labor, Premature phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Menopause, Premature Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Menopause, Premature phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ovarian Failure, Premature Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ovarian Failure, Premature phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fetal Membranes, Premature Rupture Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fetal Membranes, Premature Rupture phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

premature neuronal precursor differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature neuronal precursor differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular premature beat Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular premature beat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature suture closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature suture closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature aging Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature aging phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature closure of the ductus arteriosus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature closure of the ductus arteriosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature endochondral bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pregnancy-related premature death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pregnancy-related premature death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

?premature ovarian failure 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?premature ovarian failure 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

[premature chromatid separation trait] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [premature chromatid separation trait] phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

{preterm premature rupture of the membranes, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {preterm premature rupture of the membranes, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

premature ovarian failure Gene Set

From OMIM Gene-Disease Associations

genes associated with the premature ovarian failure phenotype from the curated OMIM Gene-Disease Associations dataset.

Male hypogonadism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Male hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CATSPER-Related Male Infertility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CATSPER-Related Male Infertility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

male pronucleus Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the male pronucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

male germ cell nucleus Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the male germ cell nucleus cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

male pronucleus Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the male pronucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

male germ cell nucleus Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the male germ cell nucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Male Urogenital Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Male Urogenital Diseases from the curated CTD Gene-Disease Associations dataset.

Infertility, Male Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Infertility, Male from the curated CTD Gene-Disease Associations dataset.

Genital Diseases, Male Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Genital Diseases, Male from the curated CTD Gene-Disease Associations dataset.

Breast Neoplasms, Male Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Breast Neoplasms, Male from the curated CTD Gene-Disease Associations dataset.

Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa from the curated CTD Gene-Disease Associations dataset.

Infertility, Male Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Infertility, Male in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

male reproductive system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease male reproductive system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

male infertility Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease male infertility in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

male reproductive system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease male reproductive system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

male reproductive organ cancer Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease male reproductive organ cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

male reproductive organ benign neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease male reproductive organ benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

male urethral cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease male urethral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

male reproductive organ cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease male reproductive organ cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

male infertility Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease male infertility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

male breast cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease male breast cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

male reproductive system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease male reproductive system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cystic fibrosis; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; urogenital abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; urogenital abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

chromosome aberrations; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; oligospermia; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; oligospermia; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nonsurvivors of sepsis (male only) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nonsurvivors of sepsis (male only) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; infertility, male; varicocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; infertility, male; varicocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; breast neoplasms, male; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult male height Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult male height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome deletion; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast cancer, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast cancer, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cryptorchidism; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cryptorchidism; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; neoplasms, prostatic; neoplasms, testis; prostatic neoplasms; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; neoplasms, prostatic; neoplasms, testis; prostatic neoplasms; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

male longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease male longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial male-limited precocious puberty. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthenozoospermia; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthenozoospermia; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

testosterone; infertility, male; hypogonadism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease testosterone; infertility, male; hypogonadism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gonadal dysgenesis, 46,xy; infertility, male; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gonadal dysgenesis, 46,xy; infertility, male; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

breast neoplasms, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; varicocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; varicocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; hypospadias; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; hypospadias; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

male breast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease male breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; breast neoplasms, male; mammary neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cystic fibrosis; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

male infertility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms, prostatic; ovarian neoplasm; ovarian neoplasms; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms, prostatic; ovarian neoplasm; ovarian neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; sertoli cell-only syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; sertoli cell-only syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemochromatosis; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hernia, inguinal; infertility, male Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hernia, inguinal; infertility, male in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

left ventricular mass in male athletes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular mass in male athletes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; oligospermia; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

male Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term male in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

POR_DELETION_GDS1093_240_mouse_Liver from male 3 month old Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the POR_DELETION_GDS1093_240_mouse_Liver from male 3 month old gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

male gamete generation Gene Set

From GO Biological Process Annotations

genes participating in the male gamete generation biological process from the curated GO Biological Process Annotations dataset.

male genitalia development Gene Set

From GO Biological Process Annotations

genes participating in the male genitalia development biological process from the curated GO Biological Process Annotations dataset.

male courtship behavior Gene Set

From GO Biological Process Annotations

genes participating in the male courtship behavior biological process from the curated GO Biological Process Annotations dataset.

positive regulation of male germ cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations dataset.

development of secondary male sexual characteristics Gene Set

From GO Biological Process Annotations

genes participating in the development of secondary male sexual characteristics biological process from the curated GO Biological Process Annotations dataset.

male germ cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the male germ cell proliferation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of male germ cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations dataset.

male meiosis i Gene Set

From GO Biological Process Annotations

genes participating in the male meiosis i biological process from the curated GO Biological Process Annotations dataset.

positive regulation of male gonad development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of male gonad development biological process from the curated GO Biological Process Annotations dataset.

male germ-line sex determination Gene Set

From GO Biological Process Annotations

genes participating in the male germ-line sex determination biological process from the curated GO Biological Process Annotations dataset.

male genitalia morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the male genitalia morphogenesis biological process from the curated GO Biological Process Annotations dataset.

male pronucleus assembly Gene Set

From GO Biological Process Annotations

genes participating in the male pronucleus assembly biological process from the curated GO Biological Process Annotations dataset.

dna demethylation of male pronucleus Gene Set

From GO Biological Process Annotations

genes participating in the dna demethylation of male pronucleus biological process from the curated GO Biological Process Annotations dataset.

regulation of male germ cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of male germ cell proliferation biological process from the curated GO Biological Process Annotations dataset.

male sex differentiation Gene Set

From GO Biological Process Annotations

genes participating in the male sex differentiation biological process from the curated GO Biological Process Annotations dataset.

male sex determination Gene Set

From GO Biological Process Annotations

genes participating in the male sex determination biological process from the curated GO Biological Process Annotations dataset.

male anatomical structure morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the male anatomical structure morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of male gonad development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of male gonad development biological process from the curated GO Biological Process Annotations dataset.

male meiosis chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the male meiosis chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

male meiosis Gene Set

From GO Biological Process Annotations

genes participating in the male meiosis biological process from the curated GO Biological Process Annotations dataset.

male meiosis chromosome separation Gene Set

From GO Biological Process Annotations

genes participating in the male meiosis chromosome separation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of male gonad development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of male gonad development biological process from the curated GO Biological Process Annotations dataset.

inter-male aggressive behavior Gene Set

From GO Biological Process Annotations

genes participating in the inter-male aggressive behavior biological process from the curated GO Biological Process Annotations dataset.

male germ-line stem cell asymmetric division Gene Set

From GO Biological Process Annotations

genes participating in the male germ-line stem cell asymmetric division biological process from the curated GO Biological Process Annotations dataset.

male gonad development Gene Set

From GO Biological Process Annotations

genes participating in the male gonad development biological process from the curated GO Biological Process Annotations dataset.

male mating behavior Gene Set

From GO Biological Process Annotations

genes participating in the male mating behavior biological process from the curated GO Biological Process Annotations dataset.

male pronucleus Gene Set

From GO Cellular Component Annotations

proteins localized to the male pronucleus cellular component from the curated GO Cellular Component Annotations dataset.

male germ cell nucleus Gene Set

From GO Cellular Component Annotations

proteins localized to the male germ cell nucleus cellular component from the curated GO Cellular Component Annotations dataset.

Male infertility Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Male infertility phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Breast cancer (male) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Breast cancer (male) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

male infertility Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease male infertility in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

male reproductive system disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease male reproductive system disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

male reproductive organ cancer Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease male reproductive organ cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

abnormality of the male genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal male reproductive system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

male infertility Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the male infertility phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of male external genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

hypoplastic male external genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplastic male external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal male reproductive system physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ambiguous genitalia, male Gene Set

From HPO Gene-Disease Associations

genes associated with the ambiguous genitalia, male phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

male hypogonadism Gene Set

From HPO Gene-Disease Associations

genes associated with the male hypogonadism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gonadal dysgenesis, male Gene Set

From HPO Gene-Disease Associations

genes associated with the gonadal dysgenesis, male phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of male internal genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of male internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

functional abnormality of male internal genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the functional abnormality of male internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the male genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the male genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

male infertility Gene Set

From HPO Gene-Disease Associations

genes associated with the male infertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal male germ cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

male pseudohermaphroditism Gene Set

From HPO Gene-Disease Associations

genes associated with the male pseudohermaphroditism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of male external genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of male external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Genital Neoplasms, Male Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Genital Neoplasms, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Infertility, Male Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infertility, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Genital Diseases, Male Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Genital Diseases, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Breast Neoplasms, Male Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Breast Neoplasms, Male phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Male Urogenital Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Male Urogenital Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

DMRT/protein doublesex/protein male abnormal 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Male sterility, NAD-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Male sterility, NAD-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Male enhanced antigen 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Male enhanced antigen 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein male abnormal 21-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein male abnormal 21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein male-specific lethal-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein male-specific lethal-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription factor homeodomain, male germ-cell Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription factor homeodomain, male germ-cell protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal male genitalia morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male urethra morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male reproductive gland physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male germ cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male germ cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

reduced male fertility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced male fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male reproductive system physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male reproductive system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male preputial gland morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male preputial gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed male fertility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed male fertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small male preputial glands Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small male preputial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male reproductive system morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male reproductive system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent external male genitalia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent external male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male prostatic urethra morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male prostatic urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

reduced male mating frequency Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced male mating frequency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent male inguinal canal Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent male inguinal canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent male preputial gland Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent male preputial gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged external male genitalia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged external male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal internal male genitalia morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal internal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal external male genitalia morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal external male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male accessory sex gland morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male accessory sex gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

submission towards male mice Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the submission towards male mice phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male inguinal canal morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male inguinal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

male infertility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the male infertility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

arrest of male meiosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the arrest of male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male meiosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small external male genitalia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small external male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent internal male genitalia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent internal male genitalia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

male pseudohermaphroditism Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the male pseudohermaphroditism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased male germ cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased male germ cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

external male genitalia atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male germ cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male germ cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal male reproductive gland morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male reproductive gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal x-y chromosome synapsis during male meiosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal x-y chromosome synapsis during male meiosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{male germ cell tumor, somatic}, 273300, Gene Set

From OMIM Gene-Disease Associations

genes associated with the {male germ cell tumor, somatic}, 273300, phenotype from the curated OMIM Gene-Disease Associations dataset.

{breast cancer, male, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {breast cancer, male, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

precocious puberty, male Gene Set

From OMIM Gene-Disease Associations

genes associated with the precocious puberty, male phenotype from the curated OMIM Gene-Disease Associations dataset.

male germ cell tumor Gene Set

From OMIM Gene-Disease Associations

genes associated with the male germ cell tumor phenotype from the curated OMIM Gene-Disease Associations dataset.

?male pseudohermaphroditism due to defective lh Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male pseudohermaphroditism due to defective lh phenotype from the curated OMIM Gene-Disease Associations dataset.

pseudohermaphroditism, male, with gynecomastia Gene Set

From OMIM Gene-Disease Associations

genes associated with the pseudohermaphroditism, male, with gynecomastia phenotype from the curated OMIM Gene-Disease Associations dataset.

?male infertility Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male infertility phenotype from the curated OMIM Gene-Disease Associations dataset.

?male infertility due to acrosin deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?male infertility due to acrosin deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

male Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term male in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Fetal Brain Male Gene Set

From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles

genes with high or low DNA methylation in Fetal Brain Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.

Skeletal Muscle Male Gene Set

From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles

genes with high or low DNA methylation in Skeletal Muscle Male 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 Male 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 Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.

internal male genital organ Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue internal male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

male reproductive system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue male reproductive system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

external male genital organ Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue external male genital organ from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

male reproductive gland Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue male reproductive gland from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

male reproductive gland Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue male reproductive gland in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

male reproductive system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue male reproductive system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

internal male genital organ Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue internal male genital organ in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

external male genital organ Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue external male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

male cone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue male cone in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

male reproductive system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue male reproductive system in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

internal male genital organ Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue internal male genital organ in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

male urethra Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue male urethra in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

male reproductive gland Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue male reproductive gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set

From Biocarta Pathways

proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.

postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety and hostility and depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamins and metabolites in pregnant women and neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

racemase and epimerase activity, acting on amino acids and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set

From Reactome Pathways

proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.

Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set

From Reactome Pathways

proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.

PI and PC transport between ER and Golgi membranes Gene Set

From Reactome Pathways

proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

From Reactome Pathways

proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.

FGFR1c and Klotho ligand binding and activation Gene Set

From Reactome Pathways

proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.

Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.

Synthesis and interconversion of nucleotide di- and triphosphates Gene Set

From Reactome Pathways

proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the Wikipathways Pathways dataset.

SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.

regulation of eif-4e and p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.

vegf hypoxia and angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.

yaci and bcma stimulation of b cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.

lck and fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.

hiv-1 nef: negative effector of fas and tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.

ucalpain and friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.

ionomycin and phorbal ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.

carm1 and regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.

phosphoinositides and their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

transcription factor creb and its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways 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.

the igf-1 receptor and longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.

cdc25 and chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.

human cytomegalovirus and map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.

influence of ras and rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

proteolysis and signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.

apoptotic dna-fragmentation and tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.

ion channels and their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

fosb gene expression and drug abuse Gene Set

From Biocarta Pathways

proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.

links between pyk2 and map kinases Gene Set

From Biocarta Pathways

proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.

opposing roles of aif in apoptosis and cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from the Biocarta Pathways dataset.

degradation of the rar and rxr by the proteasome Gene Set

From Biocarta Pathways

proteins participating in the degradation of the rar and rxr by the proteasome pathway from the Biocarta Pathways dataset.

cadmium induces dna synthesis and proliferation in macrophages Gene Set

From Biocarta Pathways

proteins participating in the cadmium induces dna synthesis and proliferation in macrophages pathway from the Biocarta Pathways dataset.

erk and pi-3 kinase are necessary for collagen binding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk and pi-3 kinase are necessary for collagen binding in corneal epithelia pathway from the Biocarta Pathways dataset.

role of brca1 brca2 and atr in cancer susceptibility Gene Set

From Biocarta Pathways

proteins participating in the role of brca1 brca2 and atr in cancer susceptibility pathway from the Biocarta Pathways dataset.

chrebp regulation by carbohydrates and camp Gene Set

From Biocarta Pathways

proteins participating in the chrebp regulation by carbohydrates and camp pathway from the Biocarta Pathways dataset.

pten dependent cell cycle arrest and apoptosis Gene Set

From Biocarta Pathways

proteins participating in the pten dependent cell cycle arrest and apoptosis pathway from the Biocarta Pathways dataset.

induction of apoptosis through dr3 and dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 and dr4/5 death receptors pathway from the Biocarta Pathways dataset.

CIITA-18437201-Raji B cells and iDC-human Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CIITA-18437201-Raji B cells and iDC-human transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

VDR-23401126-LCL-AND-THP1-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the YY1-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

BACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the BACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the EZH2-23942234-MYOBLASTS AND MYOTUBES-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Hypothyroidism, central, and testicular enlargement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, central, and testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trifunctional protein deficiency with myopathy and neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy and neuropathy 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.

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate 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.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vater association with macrocephaly and ventriculomegaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vater association with macrocephaly and ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hamartomas nephroblastomatosis and fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephroblastomatosis and fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, and sideroblastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined cellular and humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined cellular and humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined d-2- and l-2-hydroxyglutaric aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined d-2- and l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sinoatrial node dysfunction and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Warts, hypogammaglobulinemia, infections, and myelokathexis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Warts, hypogammaglobulinemia, infections, and myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia 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.

Insulin-resistant diabetes mellitus AND acanthosis nigricans Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-resistant diabetes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility 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.

Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 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.

Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous and Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory and autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal, 2 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.

Anemia sideroblastic and spinocerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infertility associated with multi-tailed spermatozoa and excessive DNA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infertility associated with multi-tailed spermatozoa and excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy 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.

Mullerian aplasia and hyperandrogenism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mullerian aplasia and hyperandrogenism 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.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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.

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multicentric osteolysis, nodulosis and arthropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multicentric osteolysis, nodulosis and arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stapes ankylosis with broad thumb and toes Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis 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.

Myopathy, lactic acidosis, and sideroblastic anemia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, and sideroblastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor and sensory, Okinawa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, short stature, and impaired glucose metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts 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.

Macrocephaly, alopecia, cutis laxa, and scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macrocephaly, alopecia, cutis laxa, and scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract 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.

Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy dilated with woolly hair and keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, renal dysfunction, and cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract and cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin and bowel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, microphthalmia and nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bone fragility with contractures, arterial rupture, and deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bone fragility with contractures, arterial rupture, and deafness 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.

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna and fibula absence of with severe limb deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ulna and fibula absence of with severe limb deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor v and factor viii, combined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor v and factor viii, combined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary Paragangliomas and Pheochromocytomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Band-like calcification with simplified gyration and polymicrogyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Band-like calcification with simplified gyration and polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercarotenemia and vitamin a deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercarotenemia and vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 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.

Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, X-linked, with variable learning disabilities and behavior disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, X-linked, with variable learning disabilities and behavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, juvenile, with microcornea and glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, juvenile, with microcornea and glucosuria 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.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, deafness, and narcolepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile macular degeneration and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary leiomyomatosis and renal cell cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monocyte and dendritic cell deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte and dendritic cell deficiency, autosomal recessive 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.

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.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 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.

Combined malonic and methylmalonic aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined malonic and methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glomerulocystic kidney disease with hyperuricemia and isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glomerulocystic kidney disease with hyperuricemia and isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis 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.

Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia, cerebellar ataxia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hereditary motor and sensory neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis and dental anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mycobacterial and viral infections, susceptibility to, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycobacterial and viral infections, susceptibility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, hyperphagia, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebroretinal microangiopathy with calcifications and cysts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy and paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI 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.

Microcephaly, normal intelligence and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Calcification of joints and arteries Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Calcification of joints and arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypotrichosis and recurrent skin vesicles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy 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.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 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.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pineal hyperplasia AND diabetes mellitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Morbid obesity and spermatogenic failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Morbid obesity and spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sensory and autonomic neuropathy type IIA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia, high, with cataract and vitreoretinal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of factor V and factor VIII, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of factor V and factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, and hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyogenic arthritis, pyoderma gangrenosum and acne Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyogenic arthritis, pyoderma gangrenosum and acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth deficiency and mental retardation with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, cochlear, with myopia and intellectual impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Combined deficiency of sialidase AND beta galactosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Combined deficiency of sialidase AND beta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

calcium- and calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the calcium- and calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mrna cleavage and polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mrna cleavage and polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial sorting and assembly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

calcium- and calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the calcium- and calmodulin-dependent protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cortical layer of collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cortical layer of collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mrna cleavage and polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mrna cleavage and polyadenylation specificity factor complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen and cuticulin-based cuticle extracellular matrix part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen and cuticulin-based cuticle extracellular matrix part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial sorting and assembly machinery complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial sorting and assembly machinery complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) Gene Set

From CORUM Protein Complexes

proteins in the TRBP containing complex (DICER, RPL7A, EIF6, MOV10 and subunits of the 60S ribosomal particle) protein complex from the CORUM Protein Complexes dataset.

NRD complex (Nucleosome remodeling and deacetylation complex) Gene Set

From CORUM Protein Complexes

proteins in the NRD complex (Nucleosome remodeling and deacetylation complex) protein complex from the CORUM Protein Complexes dataset.

6S methyltransferase and RG-containing Sm proteins complex Gene Set

From CORUM Protein Complexes

proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.

Remodeling and spacing factor (RSF) complex Gene Set

From CORUM Protein Complexes

proteins in the Remodeling and spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.

PBAF complex (Polybromo- and BAF containing complex) Gene Set

From CORUM Protein Complexes

proteins in the PBAF complex (Polybromo- and BAF containing complex) protein complex from the CORUM Protein Complexes dataset.

Cleavage and polyadenylation factor (CPSF) Gene Set

From CORUM Protein Complexes

proteins in the Cleavage and polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.

Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set

From CORUM Protein Complexes

proteins in the Apoptosis- and splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate I/200kD and III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Nucleic and chromatin Fanconi complex Gene Set

From CORUM Protein Complexes

proteins in the Nucleic and chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate V/380kD and VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set

From CORUM Protein Complexes

proteins in the Apoptosis- and splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.

ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set

From CORUM Protein Complexes

proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.

20S methylosome and RG-containing Sm protein complex Gene Set

From CORUM Protein Complexes

proteins in the 20S methylosome and RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.

Amino Acids, Peptides, and Proteins Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.

Bile Acids and Salts Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Bile Acids and Salts from the curated CTD Gene-Chemical Interactions dataset.

Prime and Bond NT Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Prime and Bond NT from the curated CTD Gene-Chemical Interactions dataset.

drospirenone and ethinyl estradiol combination Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical drospirenone and ethinyl estradiol combination from the curated CTD Gene-Chemical Interactions dataset.

Hypophosphatemic Rickets And Hyperparathyroidism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatemic Rickets And Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.

Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.

Synovitis granulomatous with uveitis and cranial neuropathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.

Hereditary Sensory and Motor Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.

Preaxial deficiency, postaxial polydactyly and hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly and hypospadias from the curated CTD Gene-Disease Associations dataset.

Combined Cellular And Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Combined Cellular And Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.

Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria and Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.

Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.

Microtia, Hearing Impairment, And Cleft Palate Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.

Acromegaloid features, overgrowth, cleft palate, and hernia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, and hernia from the curated CTD Gene-Disease Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.

Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.

Craniosynostosis, anal anomalies, and porokeratosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.

Sacral defect and anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

Classical Lissencephalies and Subcortical Band Heterotopias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Classical Lissencephalies and Subcortical Band Heterotopias from the curated CTD Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 1 and deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor and sensory, Russe type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.

Blepharophimosis, Ptosis, and Epicanthus Inversus Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blepharophimosis, Ptosis, and Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset.

Hypotrichosis And Recurrent Skin Vesicles Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.

Signs and Symptoms, Digestive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Signs and Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset.