Fetal Cardiomyopathy

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Results for "Fetal Cardiomyopathy": 1001 gene sets

Name
Fetal Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
cardiomyopathy, dilated; cardiomyopathy, hypertrophic; cardiomyopathy, restrictive; dcm - dilated cardiomyopathy; hypertrophic cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; cardiomyopathy, restrictive; dcm - dilated cardiomyopathy; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; cardiomyopathy, hypertrophic; dcm - dilated cardiomyopathy; heart failure; hypertrophic cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; dcm - dilated cardiomyopathy; heart failure; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Cardiomyopathy:Cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy:Cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
cardiomyopathy, hypertrophic; cardiomyopathy, restrictive Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; cardiomyopathy, restrictive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; coxsackievirus infections; dcm - dilated cardiomyopathy; myocarditis Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; coxsackievirus infections; dcm - dilated cardiomyopathy; myocarditis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; cardiomyopathy, dilated; dcm - dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; cardiomyopathy, dilated; dcm - dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angina pectoris; cardiomyopathy, hypertrophic; coronary artery vasospasm; coronary vasospasm; hypertrophic cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease angina pectoris; cardiomyopathy, hypertrophic; coronary artery vasospasm; coronary vasospasm; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial fibrillation; cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertension; hypertrophic cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertension; hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; cardiomyopathy, hypertrophic; Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; chagas cardiomyopathy; chagas disease; Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; chagas cardiomyopathy; chagas disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; myocardial ischemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; hemochromatosis Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; hemochromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia; postoperative complications; rheumatic heart disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia; postoperative complications; rheumatic heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease susceptibility Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Fetal Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Familial hypertrophic cardiomyopathy 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial restrictive cardiomyopathy 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial restrictive cardiomyopathy 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1LL Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1LL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Left ventricular noncompaction cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Left ventricular noncompaction cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 13 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, restrictive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, restrictive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensorineural deafness with hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensorineural deafness with hypertrophic cardiomyopathy 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.
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.
Cardiomyopathy, dilated, 2b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, dilated, 1nn Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, 1nn phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial hypertrophic cardiomyopathy 20 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial hypertrophic cardiomyopathy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1M Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1M phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, dilated, 1u Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1EE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1EE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 3B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1DD Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1DD phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arrhythmogenic right ventricular cardiomyopathy, type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular cardiomyopathy, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1S Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1W Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1W phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1X Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1X phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1Y Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1Y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1Z Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1Z phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1O Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Primary familial hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1CC Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1CC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1FF Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1FF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, hypertrophic, midventricular, digenic Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, hypertrophic, midventricular, digenic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy 1HH Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1HH phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy with left ventricular noncompaction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy with left ventricular noncompaction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy 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.
Dilated cardiomyopathy 1JJ Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dilated cardiomyopathy 1JJ phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cardiomyopathy, Restrictive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Restrictive from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 9 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 8 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 2 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 6 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Hypertrophic, Familial from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, DILATED, 3B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, DILATED, 3B from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1FF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1FF from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1DD Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1DD from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 4 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Alcoholic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Alcoholic from the curated CTD Gene-Disease Associations dataset.
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated from the curated CTD Gene-Disease Associations dataset.
Idiopathic dilation cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Idiopathic dilation cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Cataract and cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 2a Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 2a from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1K Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1K from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 3 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 3 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 10 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 13 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 13 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 15 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 15 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy dilated with Woolly hair and keratoderma Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1AA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1AA from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 1 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1C from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1D from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1E from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1J from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1N Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1N from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1M Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1M from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1V Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1V from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1g Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1g from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1i Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1i from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1o Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1o from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1s Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1s from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1p Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1p from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1q Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1q from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1w Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1w from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1u Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1u from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1z Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1z from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1x Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1x from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1y Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1y from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Restrictive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Restrictive, 2 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Hypertrophic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Hypertrophic from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 11 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1CC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1CC from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1l Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1l from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1BB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1BB from the curated CTD Gene-Disease Associations dataset.
Familial dilated cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial dilated cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease DEAFNESS, AUTOSOMAL DOMINANT 22;DFNA22 DEAFNESS, AUTOSOMAL DOMINANT 22, WITH HYPERTROPHIC CARDIOMYOPATHY, from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1t Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1t from the curated CTD Gene-Disease Associations dataset.
Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated, 1EE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Dilated, 1EE from the curated CTD Gene-Disease Associations dataset.
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12 from the curated CTD Gene-Disease Associations dataset.
Takotsubo Cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Takotsubo Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Familial Hypertrophic, 14 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy, Familial Hypertrophic, 14 from the curated CTD Gene-Disease Associations dataset.
Cardiomyopathy, Dilated Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Cardiomyopathy, Dilated in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
dilated cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dilated cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
hypertrophic cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hypertrophic cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
intrinsic cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease intrinsic cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
arrhythmogenic right ventricular cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease arrhythmogenic right ventricular cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
extrinsic cardiomyopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease extrinsic cardiomyopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
cardiomyopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cardiomyopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
dilated cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dilated cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
restrictive cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease restrictive cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
extrinsic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease extrinsic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypertrophic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypertrophic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peripartum cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripartum cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcoholic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcoholic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intrinsic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intrinsic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
arrhythmogenic right ventricular cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease arrhythmogenic right ventricular cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chagas cardiomyopathy; Gene Set From GAD Gene-Disease Associations genes associated with the disease chagas cardiomyopathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chagas cardiomyopathy; chagas disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chagas cardiomyopathy; chagas disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertrophic cardiomyopathy and cytochrome c oxidase deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophic cardiomyopathy and cytochrome c oxidase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
desmin-associated restrictive cardiomyopathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease desmin-associated restrictive cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nonfamilial idiopathic dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease nonfamilial idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; coxsackievirus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; coxsackievirus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy; heart failure Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmogenic right ventricular cardiomyopathy/dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmogenic right ventricular cardiomyopathy/dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, nonfamilial hypertrophic Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, nonfamilial hypertrophic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy; heart anomalies, congenital Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy; heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, idiopathic dilated Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, idiopathic dilated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomegaly; cardiomyopathy, dilated; Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomegaly; cardiomyopathy, dilated; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy; heart failure; sudden death Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy; heart failure; sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tachycardia cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease tachycardia cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; Gene Set From GAD Gene-Disease Associations genes associated with the disease arrhythmias, cardiac; cardiomyopathy, dilated; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertrophic cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyloid cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease amyloid cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; genetic diseases, inborn Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stress (tako-tsubo) cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease stress (tako-tsubo) cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial hypertrophic cardiomyopathy. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial hypertrophic cardiomyopathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; death, sudden, cardiac Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertrophy, left ventricular; tachycardia, ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophy, left ventricular; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hypertrophy, left ventricular Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hypertrophy, left ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chagas cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease chagas cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrial fibrillation; cardiomyopathy, dilated; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease atrial fibrillation; cardiomyopathy, dilated; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, familial Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
x-linked dilated cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease x-linked dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
takotsubo cardiomyopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease takotsubo cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic; hepatitis c Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic; hepatitis c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiomyopathy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cardiomyopathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Cardiomyopathy, Dilated_Myocardial tissue_GSE3586 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Cardiomyopathy, Dilated_Myocardial tissue_GSE3586 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Dilated cardiomyopathy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Dilated cardiomyopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Chagas cardiomyopathy in Tripanosoma cruzi seropositivity Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Chagas cardiomyopathy in Tripanosoma cruzi seropositivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
dilated cardiomyopathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease dilated cardiomyopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
peripartum cardiomyopathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease peripartum cardiomyopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
hypertrophic cardiomyopathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
intrinsic cardiomyopathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease intrinsic cardiomyopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
cardiomyopathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cardiomyopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
dilated cardiomyopathy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the dilated cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
hypertrophic cardiomyopathy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the hypertrophic cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
cardiomyopathy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the cardiomyopathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
noncompaction cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the noncompaction cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrial cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the atrial cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
restrictive cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the restrictive cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
right ventricular cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the right ventricular cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dilated cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the dilated cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypertrophic cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the hypertrophic cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
concentric hypertrophic cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the concentric hypertrophic cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
oncocytic cardiomyopathy Gene Set From HPO Gene-Disease Associations genes associated with the oncocytic cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cardiomyopathy, Restrictive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Restrictive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cardiomyopathy, Hypertrophic, Familial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Hypertrophic, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cardiomyopathy, Alcoholic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Alcoholic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Chagas Cardiomyopathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chagas Cardiomyopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cardiomyopathy, Hypertrophic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Hypertrophic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cardiomyopathy, Dilated Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cardiomyopathy, Dilated phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Takotsubo Cardiomyopathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Takotsubo Cardiomyopathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
cardiomyopathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cardiomyopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dilated cardiomyopathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dilated cardiomyopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ventricular cardiomyopathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ventricular cardiomyopathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis Gene Set From OMIM Gene-Disease Associations genes associated with the dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated 1c Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated 1c phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated 1b Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1cc Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1cc phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant 22, with hypertrophic cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant 22, with hypertrophic cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, early-onset, with fatal cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1ee Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1ee phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 2a Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 18 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 10 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 13 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 12 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 15 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 14 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 16 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic 17 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, with woolly hair and keratoderma Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, with woolly hair and keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 21 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 22 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 22 phenotype from the curated OMIM Gene-Disease Associations dataset.
?cardiomyopathy, dilated, 1aa Gene Set From OMIM Gene-Disease Associations genes associated with the ?cardiomyopathy, dilated, 1aa phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 9 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 8 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 7 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1hh Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1hh phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1jj Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1jj phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1ll Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1ll phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1nn Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1nn phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial restrictive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial restrictive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1bb Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1bb phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1dd Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1dd phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, hypertrophic, midventricular, digenic Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, hypertrophic, midventricular, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 3b Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 3b phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic phenotype from the curated OMIM Gene-Disease Associations dataset.
?cardiomyopathy, dilated, 1t Gene Set From OMIM Gene-Disease Associations genes associated with the ?cardiomyopathy, dilated, 1t phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1ff Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1ff phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1a Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1a phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1g Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1g phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1d Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1d phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1e Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1e phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1k Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1k phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1h Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1h phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1i Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1i phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1n Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1n phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1o Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1o phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1l Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1l phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1m Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1m phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1r Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1r phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1s Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1s phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1p Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1p phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1q Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1q phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1v Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1v phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1w Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1w phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1u Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1u phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1z Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1z phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1x Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1x phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1y Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1y phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1kk Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1kk phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, familial hypertrophic, 20 Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, familial hypertrophic, 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 2b Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1j Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1j phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1ii Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1ii phenotype from the curated OMIM Gene-Disease Associations dataset.
left ventricular noncompaction 3, with or without dilated cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the left ventricular noncompaction 3, with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1gg Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1gg phenotype from the curated OMIM Gene-Disease Associations dataset.
?cardiac conduction disease with or without dilated cardiomyopathy Gene Set From OMIM Gene-Disease Associations genes associated with the ?cardiac conduction disease with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
cardiomyopathy, dilated, 1mm Gene Set From OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, 1mm phenotype from the curated OMIM Gene-Disease Associations dataset.
Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Arrhythmogenic Right Ventricular Cardiomyopathy(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
ventricular tachycardia; hypertrophic cardiomyopathy Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease ventricular tachycardia; hypertrophic cardiomyopathy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
cardiomyopathy Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease cardiomyopathy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Mitochondrial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mitochondrial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypertrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ischemic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Restrictive Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Restrictive Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypertrophic Obstructive Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypertrophic Obstructive Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chagas Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chagas Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Noncompaction Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Noncompaction Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Takotsubo Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Takotsubo Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Apical Hypertrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Apical Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inflammatory Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Compaction Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Compaction Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Left Ventricular Noncompaction Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Noncompaction Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Ischemic Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Ischemic Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Danish Type Familial Amyloid Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Danish Type Familial Amyloid Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Postpartum Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Postpartum Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dilated Cardiomyopathy Secondary To Metabolic Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dilated Cardiomyopathy Secondary To Metabolic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Histiocytoid Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Histiocytoid Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dmd-Associated Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dmd-Associated Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Hypertrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Ischemic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Ischemic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Obscure African Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Obscure African Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Concentric Hypertrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Concentric Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dilated Cardiomyopathy Secondary To Viral Myocarditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dilated Cardiomyopathy Secondary To Viral Myocarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Right Ventricular Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Right Ventricular Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Restrictive Cardiomyopathy (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Restrictive Cardiomyopathy (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Restrictive Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Restrictive Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Hypertrophic Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Hypertrophic Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Valvular Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Valvular Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fatal Infantile Mitochondrial Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fatal Infantile Mitochondrial Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stress Induced Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stress Induced Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pacing-Induced Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pacing-Induced Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonobstructive Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonobstructive Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Amyloid Cardiomyopathy, Transthyretin-Related Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amyloid Cardiomyopathy, Transthyretin-Related in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transthyretin Related Familial Amyloid Cardiomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transthyretin Related Familial Amyloid Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripartum Cardiomyopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripartum Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cardiomyopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiomyopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
dilated cardiomyopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated cardiomyopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ventricular cardiomyopathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ventricular cardiomyopathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Arrhythmogenic right ventricular cardiomyopathy Gene Set From WikiPathways Pathways 2024 proteins participating in the Arrhythmogenic right ventricular cardiomyopathy pathway from the WikiPathways Pathways 2024 dataset.
Cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Intrinsic cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Intrinsic cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Dilated cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dilated cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Arrhythmogenic right ventricular cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Arrhythmogenic right ventricular cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Restrictive cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Restrictive cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hypertrophic cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Familial hypertrophic cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial hypertrophic cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked dilated cardiomyopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked dilated cardiomyopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cardiomyopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Cardiomyopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrinsic cardiomyopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Intrinsic cardiomyopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Dilated cardiomyopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intrinsic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intrinsic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile hypertrophic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile hypertrophic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arrhythmogenic right ventricular cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arrhythmogenic right ventricular cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Extrinsic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Extrinsic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peripartum cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripartum cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1EE Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1EE in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Restrictive cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Restrictive cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial hypertrophic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial hypertrophic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arrhythmogenic biventricular cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arrhythmogenic biventricular cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arrhythmogenic left ventricular cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arrhythmogenic left ventricular cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked dilated cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked dilated cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1X Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1X in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1FF Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1FF in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Restrictive cardiomyopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Restrictive cardiomyopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1HH Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1HH in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alcoholic cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alcoholic cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Restrictive cardiomyopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Restrictive cardiomyopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1H Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1H in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1KK Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1KK in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1P Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1P in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1DD Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1DD in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1GG Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1GG in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1M Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1M in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Restrictive cardiomyopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Restrictive cardiomyopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 17 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 17 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1T Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1T in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1G Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1G in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1JJ Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1JJ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile histiocytoid cardiomyopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile histiocytoid cardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1O Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1O in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 3B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 3B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy 1L Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dilated cardiomyopathy 1L in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 20 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 20 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypertrophic cardiomyopathy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypertrophic cardiomyopathy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary familial dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary familial dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arrhythmogenic right ventricular cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arrhythmogenic right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary familial hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arrhythmogenic ventricular cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arrhythmogenic ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial Hypertrophic Cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial Hypertrophic Cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial isolated dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial isolated dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial restrictive cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial restrictive cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Restrictive cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Restrictive cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intrinsic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intrinsic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Left ventricular noncompaction cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Left ventricular noncompaction cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arrhythmogenic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arrhythmogenic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyprtrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyprtrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
DSP-related arrhythmogenic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the DSP-related arrhythmogenic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Family history of cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Family history of cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ANKRD1-related dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ANKRD1-related dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial dilated cardiomyopathy and peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial dilated cardiomyopathy and peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cardiomyopathy-hypotonia-lactic acidosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cardiomyopathy-hypotonia-lactic acidosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MYH7-related cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MYH7-related cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Concentric hypertrophic cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Concentric hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Histiocytoid cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Histiocytoid cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
DSP-related cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the DSP-related cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Noncompaction cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Noncompaction cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Right ventricular cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Right ventricular cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TXNRD2-associated Cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TXNRD2-associated Cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial cardiomyopathy and sudden cardiac failure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial cardiomyopathy and sudden cardiac failure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ILK-related cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ILK-related cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-compaction cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-compaction cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant dilated cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dilated cardiomyopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Dilated cardiomyopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypertrophic cardiomyopathy (sarcomere positive) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertrophic cardiomyopathy (sarcomere positive) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypertrophic cardiomyopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertrophic cardiomyopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypertrophic cardiomyopathy (sarcomere negative) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertrophic cardiomyopathy (sarcomere negative) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Chagas cardiomyopathy in Tripanosoma cruzi seropositivity Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chagas cardiomyopathy in Tripanosoma cruzi seropositivity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypertrophic cardiomyopathy (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hypertrophic cardiomyopathy (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Dilated cardiomyopathy (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Dilated cardiomyopathy (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Idiopathic dilated cardiomyopathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic dilated cardiomyopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hypertrophic cardiomyopathy Gene Set From KEGG Pathways 2026 proteins participating in the Hypertrophic cardiomyopathy pathway from the KEGG Pathways 2026 dataset.
Arrhythmogenic right ventricular cardiomyopathy Gene Set From KEGG Pathways 2026 proteins participating in the Arrhythmogenic right ventricular cardiomyopathy pathway from the KEGG Pathways 2026 dataset.
Dilated cardiomyopathy Gene Set From KEGG Pathways 2026 proteins participating in the Dilated cardiomyopathy pathway from the KEGG Pathways 2026 dataset.
Diabetic cardiomyopathy Gene Set From KEGG Pathways 2026 proteins participating in the Diabetic cardiomyopathy pathway from the KEGG Pathways 2026 dataset.
TAL1-20566737-PRIMARY FETAL LIVER ERYTHROID CELLS-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the TAL1-20566737-PRIMARY FETAL LIVER ERYTHROID CELLS-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.
KLF1-20508144-FETAL-LIVER-ERYTHROID-MOUSE Gene Set From ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the KLF1-20508144-FETAL-LIVER-ERYTHROID-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles 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.
Fetal hemoglobin quantitative trait locus 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fetal hemoglobin quantitative trait locus 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fetal hemoglobin quantitative trait locus 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Fetal hemoglobin quantitative trait locus 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Fetal Resorption Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Resorption from the curated CTD Gene-Disease Associations dataset.
Fetal Alcohol Spectrum Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Alcohol Spectrum Disorders from the curated CTD Gene-Disease Associations dataset.
Fetal Growth Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Growth Retardation from the curated CTD Gene-Disease Associations dataset.
Fetal Weight Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Weight from the curated CTD Gene-Disease Associations dataset.
Fetal Death Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Death from the curated CTD Gene-Disease Associations dataset.
Pierre Robin syndrome with fetal chondrodysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pierre Robin syndrome with fetal chondrodysplasia from the curated CTD Gene-Disease Associations dataset.
Fetal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Diseases from the curated CTD Gene-Disease Associations dataset.
Persistent Fetal Circulation Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Persistent Fetal Circulation Syndrome from the curated CTD Gene-Disease Associations dataset.
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor from the curated CTD Gene-Disease Associations dataset.
Fetal Nutrition Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Nutrition Disorders from the curated CTD Gene-Disease Associations dataset.
Fetal Distress Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Distress from the curated CTD Gene-Disease Associations dataset.
Fetal Hemoglobin Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Fetal Hemoglobin in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
persistent fetal circulation syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease persistent fetal circulation syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial fetal alcohol syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal alcohol syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal alcohol spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal erythroblastosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal erythroblastosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal adenoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal adenoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal diseases; hemoglobinopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; hemoglobinopathies 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.
birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal nutrition disorders; hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal nutrition disorders; hypercholesterolemia 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 death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death; hyperhomocysteinemia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pregnancy loss, recurrent; fetal loss Gene Set From GAD Gene-Disease Associations genes associated with the disease pregnancy loss, recurrent; fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal hemoglobin levels Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal hemoglobin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
embryo loss; fetal death Gene Set From GAD Gene-Disease Associations genes associated with the disease embryo loss; fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; pre-eclampsia; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss, late Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss, late in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal hemoglobin Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal hemoglobin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal akinesia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal akinesia 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.
fetal death; sudden infant death Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss, early Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss, early in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
fetal growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; fetal diseases; malnutrition; starvation Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; fetal diseases; malnutrition; starvation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism Gene Set From GAD Gene-Disease Associations genes associated with the disease complication, cardiovascular pregnancy; fetal death; pregnancy complications, cardiovascular; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; hemophilia a Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; hemophilia a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss, late; pregnancy loss, recurrent Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss, late; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent early fetal loss Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent early fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal membrane rupture Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal membrane rupture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
beta thalassemia; beta-thalassemia; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; periodontal diseases; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; periodontal diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alpha thalassemia; alpha-thalassemia; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alpha thalassemia; alpha-thalassemia; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal loss ; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal loss ; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic Gene Set From GAD Gene-Disease Associations genes associated with the disease abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal death Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; hellp syndrome; intrauterine growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
recurrent fetal loss Gene Set From GAD Gene-Disease Associations genes associated with the disease recurrent fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erythroblastosis, fetal Gene Set From GAD Gene-Disease Associations genes associated with the disease erythroblastosis, fetal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal anticonvulsant syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal anticonvulsant syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; intrauterine growth retardation; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
fetal growth retardation; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
down syndrome; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease down syndrome; fetal diseases 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 growth retardation; intrauterine growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; intrauterine growth retardation 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.
fetal diseases; infection Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal diseases; infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal alcohol syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal alcohol syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal growth retardation; intrauterine growth retardation Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation 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.
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.
birth weight; fetal growth retardation; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; fetal weight; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; fetal diseases; nutrition disorders; osteoporosis; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; hellp syndrome; pre-eclampsia Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; hellp syndrome; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term fetal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Zfp36l2_deficiency_GDS3574_153_mouse_E14.5 fetal liver Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Zfp36l2_deficiency_GDS3574_153_mouse_E14.5 fetal liver gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
E2A_KO_GSE43224_679_mouse_DN2 cells from WT and E2A-deficient murine fetal thymi Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the E2A_KO_GSE43224_679_mouse_DN2 cells from WT and E2A-deficient murine fetal thymi gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
fetal process involved in parturition Gene Set From GO Biological Process Annotations 2015 genes participating in the fetal process involved in parturition biological process from the curated GO Biological Process Annotations 2015 dataset.
Fetal hemoglobin levels Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Fetal hemoglobin levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
fetal polyuria Gene Set From HPO Gene-Disease Associations genes associated with the fetal polyuria phenotype by mapping known disease genes to disease phenotypes from the HPO 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.
abnormality of the fetal cardiovascular system Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the fetal cardiovascular system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal ultrasound soft marker Gene Set From HPO Gene-Disease Associations genes associated with the fetal ultrasound soft marker phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fetal movement Gene Set From HPO Gene-Disease Associations genes associated with the decreased fetal movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal akinesia sequence Gene Set From HPO Gene-Disease Associations genes associated with the fetal akinesia sequence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal ascites Gene Set From HPO Gene-Disease Associations genes associated with the fetal ascites phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal cystic hygroma Gene Set From HPO Gene-Disease Associations genes associated with the fetal cystic hygroma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fetal megacystis Gene Set From HPO Gene-Disease Associations genes associated with the fetal megacystis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Fetal Macrosomia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Macrosomia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Persistent Fetal Circulation Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Persistent Fetal Circulation Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Weight Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Weight phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Death Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Death phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Alcohol Syndrome Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Alcohol Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Erythroblastosis, Fetal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Erythroblastosis, Fetal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Fetal Growth Retardation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Growth Retardation 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.
Fetal Nutrition Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Fetal Nutrition Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal fetal derived definitive erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lethality throughout fetal growth and development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lethality throughout fetal growth and development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal growth/weight/body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal atrioventricular canal septation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal atrioventricular canal septation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal cardiomyocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal atrioventricular canal morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal atrioventricular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal cardiomyocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete lethality throughout fetal growth and development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality throughout fetal growth and development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fetal growth retardation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fetal growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal cardiomyocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal cardiomyocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal embryonic/fetal subventricular zone morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic/fetal subventricular zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fetal bleb Gene Set From MPO Gene-Phenotype Associations gene mutations causing the fetal bleb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal cardiomyocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal derived definitive erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal placenta fetal blood space morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta fetal blood space morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal ductus arteriosus morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal ductus arteriosus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent fetal ductus arteriosus Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent fetal ductus arteriosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal liver hematopoietic progenitor cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal liver hematopoietic progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal cardiomyocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal cardiomyocyte morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal derived definitive erythrocyte morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
partial lethality throughout fetal growth and development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the partial lethality throughout fetal growth and development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal fetal cardiomyocyte physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal cardiomyocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased fetal derived definitive erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
fetal akinesia deformation sequence Gene Set From OMIM Gene-Disease Associations genes associated with the fetal akinesia deformation sequence phenotype from the curated OMIM Gene-Disease Associations dataset.
?fetal hydantoin syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ?fetal hydantoin syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
fetal hemoglobin quantitative trait locus 2 Gene Set From OMIM Gene-Disease Associations genes associated with the fetal hemoglobin quantitative trait locus 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
fetal hemoglobin quantitative trait locus 4 Gene Set From OMIM Gene-Disease Associations genes associated with the fetal hemoglobin quantitative trait locus 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
[hereditary persistence of fetal hemoglobin] Gene Set From OMIM Gene-Disease Associations genes associated with the [hereditary persistence of fetal hemoglobin] phenotype from the curated OMIM Gene-Disease Associations dataset.
fetal hemoglobin quantitative trait locus 1 Gene Set From OMIM Gene-Disease Associations genes associated with the fetal hemoglobin quantitative trait locus 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary persistence of fetal hemoglobin Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary persistence of fetal hemoglobin phenotype from the curated OMIM Gene-Disease Associations dataset.
fetal Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term fetal in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Fetal Heart Gene Set From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Fetal Heart relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles 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.
Fetal Lung Gene Set From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Fetal Lung relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.
Fetal Kidney Gene Set From Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Fetal Kidney relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset.
fetal cell line Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue fetal cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
fetal membrane Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue fetal membrane from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
fetal serum Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fetal serum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
fetal cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fetal cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
fetal membrane Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue fetal membrane in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Fetal growth restriction Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease Fetal growth restriction from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Fetal Resorption Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Resorption in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Persistent Fetal Circulation Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Persistent Fetal Circulation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Distress Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Distress in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Megacystis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Megacystis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Alcohol Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Alcohol Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Anemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Anemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Abnormality Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Ascites Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Ascites in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Fetal Alcohol Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Fetal Alcohol Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Persistence Of Fetal Hemoglobin Thalassemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Persistence Of Fetal Hemoglobin Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Anencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Anencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Hypoxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Hypoxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intrapartum Fetal Hypoxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intrapartum Fetal Hypoxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Pyelectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Pyelectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Cerebral Ventriculomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Cerebral Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Persistent Fetal Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Persistent Fetal Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Hydantoin Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Hydantoin Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Adenocarcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Lung Adenocarcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Lung Adenocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nephroblastomatosis, Fetal Ascites, Macrosomia And Wilms Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nephroblastomatosis, Fetal Ascites, Macrosomia And Wilms Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Rhabdomyoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Rhabdomyoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Preterm Premature Rupture Of Fetal Membranes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Preterm Premature Rupture Of Fetal Membranes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Fetal Ventriculomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Fetal Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Malnutrition Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Malnutrition in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Malnutrition Without Mention Of Light-For-Dates Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Malnutrition Without Mention Of Light-For-Dates in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Thrombotic Vasculopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Thrombotic Vasculopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Macrosomia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Macrosomia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Fetal Pyelectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Fetal Pyelectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Nutrition Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Nutrition Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Microcephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Heart Failure Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fetal Heart Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Reduced Fetal Movement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Fetal Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Membranes, Premature Rupture Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Membranes, Premature Rupture in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Severe Fetal Akinesia Sequence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Severe Fetal Akinesia Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Hemoglobin Determination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Hemoglobin Determination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Polyuria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Polyuria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Hydrops (In Some Patients) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Hydrops (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absence Of Stomach Bubble On Fetal Sonography Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absence Of Stomach Bubble On Fetal Sonography in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Premature Birth Following Premature Rupture Of Fetal Membranes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Birth Following Premature Rupture Of Fetal Membranes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Hydrops (In Perinatal Or Congenital Neuromuscular Forms) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Hydrops (In Perinatal Or Congenital Neuromuscular Forms) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Holoprosencephaly With Fetal Akinesia-Hypokinesia Sequence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Holoprosencephaly With Fetal Akinesia-Hypokinesia Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Mummification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Mummification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Hemoglobin Quantitative Trait Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Hemoglobin Quantitative Trait in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fetal Descent Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fetal Descent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Fetal Femur Length Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Fetal Femur Length in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
DMRT1-21621532-FETAL-OVARY Gene Set From ChEA Transcription Factor Targets 2022 target genes of the DMRT1-21621532-FETAL-OVARY transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
CTNNB1-20615089-FETAL-BRAIN-HUMAN Gene Set From ChEA Transcription Factor Targets 2022 target genes of the CTNNB1-20615089-FETAL-BRAIN-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
KLF1-20508144-FETAL-LIVER-ERYTHROID-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the KLF1-20508144-FETAL-LIVER-ERYTHROID-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
TAL1-20566737-PRIMARY-FETAL-LIVER-ERYTHROID-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the TAL1-20566737-PRIMARY-FETAL-LIVER-ERYTHROID-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
decreased fetal weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality throughout fetal growth and development, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality throughout fetal growth and development, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased fetal size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal atrioventricular canal morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal atrioventricular canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal cardiomyocyte morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal cardiomyocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality throughout fetal growth and development, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality throughout fetal growth and development, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fetal growth retardation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fetal growth retardation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
fetal bleb Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the fetal bleb phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal cardiomyocyte proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal cardiomyocyte proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal embryonic/fetal subventricular zone morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryonic/fetal subventricular zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal placenta fetal blood space morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placenta fetal blood space morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal growth/weight/body size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal growth/weight/body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal Leydig cell differentiation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal Leydig cell differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased fetal derived definitive erythrocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased fetal cardiomyocyte proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal derived definitive erythrocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent fetal ductus arteriosus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent fetal ductus arteriosus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal cardiomyocyte apoptosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal cardiomyocyte apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal ductus arteriosus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal ductus arteriosus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal derived definitive erythrocyte cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning, incomplete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning, incomplete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal liver hematopoietic progenitor cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal liver hematopoietic progenitor cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased fetal cardiomyocyte proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal cardiomyocyte physiology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal cardiomyocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality throughout fetal growth and development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality throughout fetal growth and development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal fetal derived definitive erythrocyte morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal derived definitive erythrocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Human - Fetal Development - L1 - Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Ganglion cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Ganglion cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Adrenocortical cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Adrenocortical cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Bronchiolar and alveolar epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Bronchiolar and alveolar epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - STC2_TLX1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - STC2_TLX1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Satellite cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Satellite cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Astrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Sympathoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Sympathoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Ureteric bud cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Ureteric bud cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Microglia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Limbic system neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Limbic system neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Inhibitory interneurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Inhibitory interneurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Chromaffin cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Chromaffin cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Oligodendrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Oligodendrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Endocardial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Endocardial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Photoreceptor cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Photoreceptor cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - ENS glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Skeletal muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - SLC24A4_PEX5L positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - SLC24A4_PEX5L positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Excitatory neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Excitatory neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Retinal progenitors and Muller glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - SKOR2_NPSR1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - SKOR2_NPSR1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Hepatoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Hepatoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Thymocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Thymocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Purkinje neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Purkinje neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Syncytiotrophoblasts and villous cytotrophoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Syncytiotrophoblasts and villous cytotrophoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Mesangial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Mesangial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Intestinal epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Intestinal epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Granule neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Granule neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Horizontal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Horizontal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Inhibitory neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Inhibitory neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Schwann cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Schwann cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Islet endocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Islet endocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Amacrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Amacrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Unipolar brush cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Unipolar brush cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - MUC13_DMBT1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - MUC13_DMBT1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Acinar cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Acinar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Metanephric cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Metanephric cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Ductal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Ductal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Retinal pigment cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Cardiomyocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Cardiomyocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Squamous epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Squamous epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Goblet cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Goblet cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Extravillous trophoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Extravillous trophoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - ENS neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Visceral neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Visceral neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Ciliated epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Ciliated epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Epicardial fat cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Epicardial fat cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Parietal and chief cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Parietal and chief cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Stellate cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Stellate cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - IGFBP1_DKK1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - IGFBP1_DKK1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Bipolar cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Bipolar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Neuroendocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Neuroendocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - PAEP_MECOM positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - PAEP_MECOM positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Corneal and conjunctival epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Corneal and conjunctival epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Hematopoietic stem cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Hematopoietic stem cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - CSH1_CSH2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - CSH1_CSH2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Lens fibre cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Lens fibre cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - CCL19_CCL21 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - CCL19_CCL21 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Trophoblast giant cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Trophoblast giant cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - SLC26A4_PAEP positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - SLC26A4_PAEP positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - AFP_ALB positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - AFP_ALB positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Thymic epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Thymic epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - PDE11A_FAM19A2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - PDE11A_FAM19A2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - Antigen presenting cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - Antigen presenting cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - SATB2_LRRC7 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - SATB2_LRRC7 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - ELF3_AGBL2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - ELF3_AGBL2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - CLC_IL5RA positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - CLC_IL5RA positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L1 - PDE1C_ACSM3 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L1 - PDE1C_ACSM3 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Ganglion cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Ganglion cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Stromal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Stromal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Adrenocortical cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Adrenocortical cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Lymphatic endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Lymphatic endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Myeloid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Myeloid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Bronchiolar and alveolar epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Bronchiolar and alveolar epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Vascular endothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Vascular endothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-STC2_TLX1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-STC2_TLX1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Satellite cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Satellite cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Astrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Astrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Astrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Astrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Sympathoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Sympathoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Ureteric bud cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Ureteric bud cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Microglia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Microglia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Microglia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Microglia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Limbic system neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Limbic system neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Inhibitory interneurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Inhibitory interneurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Chromaffin cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Chromaffin cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Chromaffin cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Chromaffin cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Oligodendrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Oligodendrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Oligodendrocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Oligodendrocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Endocardial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Endocardial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Photoreceptor cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Photoreceptor cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-ENS glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-ENS glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-ENS glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-ENS glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Lymphoid cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Lymphoid cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Skeletal muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Skeletal muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Mesothelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Mesothelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-SLC24A4_PEX5L positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-SLC24A4_PEX5L positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Excitatory neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Excitatory neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal progenitors and Muller glia cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-SKOR2_NPSR1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-SKOR2_NPSR1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Hepatoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Hepatoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Thymocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Thymocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Purkinje neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Purkinje neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Syncytiotrophoblasts and villous cytotrophoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Syncytiotrophoblasts and villous cytotrophoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Mesangial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Mesangial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Smooth muscle cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-Intestinal epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-Intestinal epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Granule neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Granule neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Horizontal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Horizontal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Inhibitory neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Inhibitory neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Schwann cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Schwann cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Muscle-Schwann cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Schwann cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-Schwann cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-Schwann cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Islet endocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Islet endocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Amacrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Amacrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebellum-Unipolar brush cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebellum-Unipolar brush cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-MUC13_DMBT1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-MUC13_DMBT1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Acinar cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Acinar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Kidney-Metanephric cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Kidney-Metanephric cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-Ductal cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-Ductal cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Retinal pigment cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Retinal pigment cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Cardiomyocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Cardiomyocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Squamous epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Squamous epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Squamous epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Squamous epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Goblet cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Goblet cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Extravillous trophoblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Extravillous trophoblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-ENS neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Intestine-ENS neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Intestine-ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-ENS neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-ENS neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Visceral neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Visceral neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Visceral neurons Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Visceral neurons cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Ciliated epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Ciliated epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Ciliated epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Ciliated epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Epicardial fat cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Epicardial fat cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Parietal and chief cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Parietal and chief cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Stellate cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Stellate cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-IGFBP1_DKK1 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-IGFBP1_DKK1 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Bipolar cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Bipolar cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-Neuroendocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-Neuroendocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-Neuroendocrine cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-Neuroendocrine cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-PAEP_MECOM positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-PAEP_MECOM positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Corneal and conjunctival epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Corneal and conjunctival epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Liver-Hematopoietic stem cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Liver-Hematopoietic stem cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-CSH1_CSH2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-CSH1_CSH2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-Lens fibre cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-Lens fibre cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Pancreas-CCL19_CCL21 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Pancreas-CCL19_CCL21 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-Trophoblast giant cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-Trophoblast giant cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Adrenal-SLC26A4_PAEP positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Adrenal-SLC26A4_PAEP positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Placenta-AFP_ALB positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Placenta-AFP_ALB positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Spleen-AFP_ALB positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Spleen-AFP_ALB positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Thymic epithelial cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Thymic epithelial cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Eye-PDE11A_FAM19A2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Eye-PDE11A_FAM19A2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Thymus-Antigen presenting cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Thymus-Antigen presenting cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-SATB2_LRRC7 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-SATB2_LRRC7 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-ELF3_AGBL2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-ELF3_AGBL2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-CLC_IL5RA positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-CLC_IL5RA positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Stomach-PDE1C_ACSM3 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Stomach-PDE1C_ACSM3 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Cerebrum-Megakaryocytes Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Cerebrum-Megakaryocytes cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Heart-Erythroblasts Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Heart-Erythroblasts cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Fetal Development - L2 - Lung-CSH1_CSH2 positive cells Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Lung-CSH1_CSH2 positive cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Circulating fetal cell_Peripheral blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Circulating fetal cell_Peripheral blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Circulating fetal cell_Blood_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Circulating fetal cell_Blood_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Retinoid acid signaling-responsive fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Retinoid acid signaling-responsive fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Oogenesis phase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Oogenesis phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Meiotic prophase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Meiotic prophase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Mitotic arrest phase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Mitotic arrest phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Mitotic fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Mitotic fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Migration phase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Migration phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Gonadal mitotic phase fetal germ cell_Fetal gonad_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Gonadal mitotic phase fetal germ cell_Fetal gonad_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Fetal hepatocyte_Liver_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Fetal hepatocyte_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Fetal hepatocyte_Liver_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Fetal hepatocyte_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Fetal myoblast_Muscle_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Fetal myoblast_Muscle_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Harmonizome 3.0

Fetal Cardiomyopathy Gene Set

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; cardiomyopathy, restrictive; dcm - dilated cardiomyopathy; hypertrophic cardiomyopathy Gene Set

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; dcm - dilated cardiomyopathy; heart failure; hypertrophic cardiomyopathy Gene Set

birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set

Cardiomyopathy:Cardiomyopathy Gene Set

Cardiomyopathy:Familial hypertrophic cardiomyopathy 4 Gene Set

cardiomyopathy, hypertrophic; cardiomyopathy, restrictive Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; tachycardia, ventricular Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; ventricular remodeling Gene Set

cardiomyopathy, dilated; coxsackievirus infections; dcm - dilated cardiomyopathy; myocarditis Gene Set

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

autoimmune diseases; cardiomyopathy, dilated; dcm - dilated cardiomyopathy Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease progression Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; death, sudden, cardiac; sudden cardiac death Gene Set

angina pectoris; cardiomyopathy, hypertrophic; coronary artery vasospasm; coronary vasospasm; hypertrophic cardiomyopathy Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left Gene Set

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies Gene Set

atrial fibrillation; cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy Gene Set

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy Gene Set

cardiomyopathy, hypertrophic; hypertension; hypertrophic cardiomyopathy Gene Set

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; Gene Set

cardiomyopathy, dilated; chagas cardiomyopathy; chagas disease; Gene Set

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; myocardial ischemia Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; hemochromatosis Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; myocardial ischemia; postoperative complications; rheumatic heart disease Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; disease susceptibility Gene Set

cardiomyopathy, hypertrophic; death, sudden, cardiac; hypertrophic cardiomyopathy; sudden cardiac death Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy Gene Set

cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure Gene Set

Fetal Dilated Cardiomyopathy Gene Set

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set

fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set

abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set

fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

Familial hypertrophic cardiomyopathy 9 Gene Set

Familial hypertrophic cardiomyopathy 7 Gene Set

Familial hypertrophic cardiomyopathy 6 Gene Set

Familial hypertrophic cardiomyopathy 4 Gene Set

Familial hypertrophic cardiomyopathy 3 Gene Set

Familial hypertrophic cardiomyopathy 2 Gene Set

Familial hypertrophic cardiomyopathy 1 Gene Set

Familial restrictive cardiomyopathy 1 Gene Set

Familial cardiomyopathy Gene Set

Dilated cardiomyopathy 1LL Gene Set

Primary dilated cardiomyopathy Gene Set

Left ventricular noncompaction cardiomyopathy Gene Set

Familial hypertrophic cardiomyopathy 17 Gene Set

Familial hypertrophic cardiomyopathy 15 Gene Set

Familial hypertrophic cardiomyopathy 14 Gene Set

Familial hypertrophic cardiomyopathy 13 Gene Set

Familial hypertrophic cardiomyopathy 12 Gene Set

Familial hypertrophic cardiomyopathy 10 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 9 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 8 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 11 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 10 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 12 Gene Set

Cardiomyopathy, restrictive Gene Set

Sensorineural deafness with hypertrophic cardiomyopathy Gene Set

Cardiomyopathy dilated with woolly hair and keratoderma Gene Set

Cataract and cardiomyopathy Gene Set

Cardiomyopathy, dilated, 2b Gene Set

Cardiomyopathy, dilated, 1nn Gene Set

Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set

Familial hypertrophic cardiomyopathy 20 Gene Set

Dilated cardiomyopathy 1C Gene Set

Dilated cardiomyopathy 1M Gene Set

Dilated cardiomyopathy 1N Gene Set

Arrhythmogenic right ventricular cardiomyopathy Gene Set

Cardiomyopathy, dilated, 1u Gene Set

Dilated cardiomyopathy 1EE Gene Set

Dilated cardiomyopathy 3B Gene Set

Dilated cardiomyopathy 1DD Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 1 Gene Set

Arrhythmogenic right ventricular cardiomyopathy, type 2 Gene Set