Name

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.

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.

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.

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.

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.

abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; 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.

abortion, habitual; abruptio placentae; activated protein c resistance; placenta abruptio; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; abruptio placentae; activated protein c resistance; placenta abruptio; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; abruptio placentae; placenta abruptio Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; abruptio placentae; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

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.

abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; activated protein c resistance; placenta abruptio; pregnancy complications, hematologic; recurrence; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; activated protein c resistance; placenta abruptio; pregnancy complications, hematologic; recurrence; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; placenta abruptio Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; placenta abruptio; pregnancy complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; placenta abruptio; pregnancy complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; placenta abruptio; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; placenta abruptio; thrombophilia 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 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.

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.

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.

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.

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 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 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.

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 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.

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.

abortion, habitual; abortion, spontaneous; obstetric labor complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; abortion, spontaneous; obstetric labor complications; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; abortion, spontaneous Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; abortion, spontaneous; autoimmune diseases Gene Set

From GAD Gene-Disease Associations

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

Abruptio Placentae Gene Set

From CTD Gene-Disease Associations

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

abruptio placentae; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abruptio placentae Gene Set

From GAD Gene-Disease Associations

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

abruptio placentae; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

preeclampsia; abruptio placentae Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; abruptio placentae in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; Gene Set

From GAD Gene-Disease Associations

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

Abruptio Placentae Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

{abruptio placentae, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {abruptio placentae, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden; death, sudden, cardiac; sudden cardiac death 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.

Abortion, Spontaneous Gene Set

From CTD Gene-Disease Associations

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

abortion, spontaneous; premature birth Gene Set

From GAD Gene-Disease Associations

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

spontaneous abortion Gene Set

From GAD Gene-Disease Associations

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

recurrent spontaneous abortion Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion, spontaneous; thrombosis Gene Set

From GAD Gene-Disease Associations

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

spontaneous abortion Gene Set

From HPO Gene-Disease Associations

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

recurrent spontaneous abortion Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent spontaneous abortion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Abortion, Spontaneous Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

intrauterine growth retardation Gene Set

From GAD Gene-Disease Associations

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

mild intrauterine growth retardation Gene Set

From HPO Gene-Disease Associations

genes associated with the mild intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intrauterine growth retardation Gene Set

From HPO Gene-Disease Associations

genes associated with the intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe intrauterine growth retardation Gene Set

From HPO Gene-Disease Associations

genes associated with the severe intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.

preeclampsia; intrauterine growth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; intrauterine growth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intrauterine growth Gene Set

From GAD Gene-Disease Associations

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

intrauterine growth restriction Gene Set

From GAD Gene-Disease Associations

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

intrauterine growth; obesity; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intrauterine growth; obesity; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease 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.

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.

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 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.

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.

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.

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.

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.

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.

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 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 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.

death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; heart diseases; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; heart diseases; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; myocardial ischemia; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; myocardial ischemia; sudden cardiac death 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.

death, sudden; sudden infant death Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; heart failure; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; death, sudden, cardiac; kidney failure, chronic; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; diabetes mellitus; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; diabetes mellitus; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; brugada syndrome; cardiomyopathies; channelopathies; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; myocardial infarction; sudden cardiac death 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.

anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD 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.

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.

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.

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.

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 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 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.

growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM 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.

placentae Gene Set

From GeneRIF Biological Term Annotations

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

intrauterine Gene Set

From GeneRIF Biological Term Annotations

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

Abortion, Threatened Gene Set

From CTD Gene-Disease Associations

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

Abortion, Habitual Gene Set

From CTD Gene-Disease Associations

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

abortion, habitual; pregnancy complications Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; infertility, female Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; infertility; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; activated protein c resistance; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; activated protein c resistance; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pregnancy complications; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; activated protein c resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; activated protein c resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; recurrence Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; activated protein c resistance; infertility, female; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; hyperhomocysteinemia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; hyperhomocysteinemia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; embryo loss; infertility, female Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; embryo loss; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; pregnancy complications, hematologic; thrombosis Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abortion Gene Set

From GeneRIF Biological Term Annotations

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

Abortion, Missed Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Abortion, Habitual Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

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.

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.

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.

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.

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.

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.

Pneumothorax, primary spontaneous Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pneumothorax, primary spontaneous phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pneumothorax, Primary Spontaneous Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pneumothorax, Primary Spontaneous from the curated CTD Gene-Disease Associations dataset.

spontaneous ocular nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

placental abruption Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hepatitis b; hepatitis b, chronic; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis b; hepatitis b, chronic; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical artery dissection, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cervical artery dissection, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

remission, spontaneous; retinopathy of prematurity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease remission, spontaneous; retinopathy of prematurity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spontaneous preterm birth Gene Set

From GAD Gene-Disease Associations

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

spontaneous chromosomal instability Gene Set

From GAD Gene-Disease Associations

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

recurrent spontaneous miscarriages Gene Set

From GAD Gene-Disease Associations

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

acute coronary syndrome; coronary artery disease; rupture, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; coronary artery disease; rupture, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c, chronic; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c, chronic; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

placental abruption Gene Set

From GAD Gene-Disease Associations

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

fractures, spontaneous; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spontaneous preterm delivery. Gene Set

From GAD Gene-Disease Associations

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

body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis b, chronic; remission, spontaneous Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis b, chronic; remission, spontaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio Gene Set

From GeneRIF Biological Term Annotations

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

abruption Gene Set

From GeneRIF Biological Term Annotations

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

spontaneous Gene Set

From GeneRIF Biological Term Annotations

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

abruptionassociated Gene Set

From GeneRIF Biological Term Annotations

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

lack of spontaneous play Gene Set

From HPO Gene-Disease Associations

genes associated with the lack of spontaneous play phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous pneumothorax Gene Set

From HPO Gene-Disease Associations

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

spontaneous esophageal perforation Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous esophageal perforation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous hematomas Gene Set

From HPO Gene-Disease Associations

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

spontaneous, recurrent epistaxis Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous, recurrent epistaxis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous neonatal pneumothorax Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous neonatal pneumothorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spontaneous hemolytic crises Gene Set

From HPO Gene-Disease Associations

genes associated with the spontaneous hemolytic crises phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Fractures, Spontaneous Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Rupture, Spontaneous Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

spontaneous chromosome breakage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spontaneous chromosome breakage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spontaneous skin ulceration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spontaneous skin ulceration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

no spontaneous movement Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the no spontaneous movement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{placental abruption} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {placental abruption} phenotype from the curated OMIM Gene-Disease Associations dataset.

pneumothorax, primary spontaneous Gene Set

From OMIM Gene-Disease Associations

genes associated with the pneumothorax, primary spontaneous phenotype from the curated OMIM Gene-Disease Associations dataset.

Placenta Gene Set

From BioGPS Human Cell Type and Tissue Gene Expression Profiles

genes with high or low expression in Placenta relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.

placenta Gene Set

From BioGPS Mouse Cell Type and Tissue Gene Expression Profiles

genes with high or low expression in placenta relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.

Placenta Diseases Gene Set

From CTD Gene-Disease Associations

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

placenta praevia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

placenta disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

placenta cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

placenta accreta Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

malaria, falciparum; placenta diseases; pregnancy complications, parasitic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, falciparum; placenta diseases; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; placenta diseases; premature birth; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

placenta diseases; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

placenta diseases Gene Set

From GAD Gene-Disease Associations

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

malaria, falciparum; parasitemia; placenta diseases; pregnancy complications, parasitic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, falciparum; parasitemia; placenta diseases; pregnancy complications, parasitic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

placenta Gene Set

From GeneRIF Biological Term Annotations

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

embryonic placenta development Gene Set

From GO Biological Process Annotations

genes participating in the embryonic placenta development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cell differentiation involved in embryonic placenta development Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cell differentiation involved in embryonic placenta development biological process from the curated GO Biological Process Annotations dataset.

regulation of cell proliferation involved in embryonic placenta development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cell proliferation involved in embryonic placenta development biological process from the curated GO Biological Process Annotations dataset.

regulation of cell differentiation involved in embryonic placenta development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cell differentiation involved in embryonic placenta development biological process from the curated GO Biological Process Annotations dataset.

maternal placenta development Gene Set

From GO Biological Process Annotations

genes participating in the maternal placenta development biological process from the curated GO Biological Process Annotations dataset.

placenta blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the placenta blood vessel development biological process from the curated GO Biological Process Annotations dataset.

embryonic placenta morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the embryonic placenta morphogenesis biological process from the curated GO Biological Process Annotations dataset.

placenta development Gene Set

From GO Biological Process Annotations

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

glycogen cell differentiation involved in embryonic placenta development Gene Set

From GO Biological Process Annotations

genes participating in the glycogen cell differentiation involved in embryonic placenta development biological process from the curated GO Biological Process Annotations dataset.

cell differentiation involved in embryonic placenta development Gene Set

From GO Biological Process Annotations

genes participating in the cell differentiation involved in embryonic placenta development biological process from the curated GO Biological Process Annotations dataset.

placenta disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormalities of placenta or umbilical cord Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormalities of placenta or umbilical cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the placenta Gene Set

From GWASdb SNP-Phenotype Associations

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

placenta Gene Set

From HPA Tissue Gene Expression Profiles

genes with high or low expression in placenta relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.

placenta Gene Set

From HPA Tissue Protein Expression Profiles

proteins with high or low expression in placenta relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.

large placenta Gene Set

From HPO Gene-Disease Associations

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

hydropic placenta Gene Set

From HPO Gene-Disease Associations

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

small placenta Gene Set

From HPO Gene-Disease Associations

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

abnormalities of placenta or umbilical cord Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormalities of placenta or umbilical cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the placenta Gene Set

From HPO Gene-Disease Associations

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

Placenta Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Placenta-expressed transcript 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Placenta-expressed transcript 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Placenta-specific protein 9 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Placenta-specific protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal placenta size Gene Set

From MPO Gene-Phenotype Associations

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

enlarged placenta Gene Set

From MPO Gene-Phenotype Associations

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

abnormal placenta hemotrichorial membrane morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal placenta hemotrichorial membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta labyrinth size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal placenta labyrinth size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal placenta development Gene Set

From MPO Gene-Phenotype Associations

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

increased placenta apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased placenta apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent placenta hemotrichorial membrane Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent placenta hemotrichorial membrane phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased placenta weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased placenta weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased placenta weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased placenta weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin placenta labyrinth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin placenta labyrinth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta metrial gland morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal placenta intervillous maternal lacunae morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal placenta intervillous maternal lacunae morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta physiology Gene Set

From MPO Gene-Phenotype Associations

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

small placenta Gene Set

From MPO Gene-Phenotype Associations

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

increased placenta intervillous maternal lacunae size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased placenta intervillous maternal lacunae size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thick placenta labyrinth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thick placenta labyrinth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent placenta Gene Set

From MPO Gene-Phenotype Associations

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

abnormal placenta vasculature Gene Set

From MPO Gene-Phenotype Associations

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

pale placenta Gene Set

From MPO Gene-Phenotype Associations

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

abnormal placenta junctional zone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal placenta junctional zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta weight Gene Set

From MPO Gene-Phenotype Associations

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

abnormal placenta labyrinth morphology Gene Set

From MPO Gene-Phenotype Associations

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

placenta Gene Set

From ProteomicsDB Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in placenta relative to other cell types and tissues from the ProteomicsDB Cell Type and Tissue Protein Expression Profiles dataset.

placenta Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

placenta Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

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

placenta Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Iron metabolism in placenta(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Iron metabolism in placenta(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Growth deficiency and mental retardation with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

mild postnatal growth retardation Gene Set

From HPO Gene-Disease Associations

genes associated with the mild postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

postnatal growth retardation Gene Set

From HPO Gene-Disease Associations

genes associated with the postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe postnatal growth retardation Gene Set

From HPO Gene-Disease Associations

genes associated with the severe postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

prenatal growth retardation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the prenatal growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

growth retardation of incisors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the growth retardation of incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

growth retardation of molars Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the growth retardation of molars phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

postnatal growth retardation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the postnatal growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

embryonic growth retardation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the embryonic growth retardation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

mental retardation, x-linked, with isolated growth hormone deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with isolated growth hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated OMIM Gene-Disease Associations dataset.

insulin-like growth factor-1; insulin-like growth factor-3 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin-like growth factor-1; insulin-like growth factor-3 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

growth plate cartilage chondrocyte growth Gene Set

From GO Biological Process Annotations

genes participating in the growth plate cartilage chondrocyte growth biological process from the curated GO Biological Process Annotations dataset.

Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) Gene Set

From Reactome Pathways

proteins participating in the Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) pathway from the Reactome Pathways dataset.

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

From Biocarta Pathways

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

Sudden cardiac death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sudden cardiac death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sudden infant death syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sudden infant death syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

death-inducing signaling complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cd95 death-inducing signaling complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cd95 death-inducing signaling complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cd95 death-inducing signaling complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cd95 death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

death-inducing signaling complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

trail death-inducing signaling complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the trail death-inducing signaling complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced Gene Set

From CORUM Protein Complexes

proteins in the Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced protein complex from the CORUM Protein Complexes dataset.

Death-inducing signaling complex DISC (type I cells associated), stimulated Gene Set

From CORUM Protein Complexes

proteins in the Death-inducing signaling complex DISC (type I cells associated), stimulated protein complex from the CORUM Protein Complexes dataset.

Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced Gene Set

From CORUM Protein Complexes

proteins in the Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced protein complex from the CORUM Protein Complexes dataset.

Death Gene Set

From CTD Gene-Disease Associations

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

Death, Sudden, Cardiac Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Death, Sudden, Cardiac from the curated CTD Gene-Disease Associations dataset.

Death, Sudden Gene Set

From CTD Gene-Disease Associations

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

Sudden Infant Death with Dysgenesis of the Testes Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sudden Infant Death with Dysgenesis of the Testes Syndrome from the curated CTD Gene-Disease Associations dataset.

Sudden Infant Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sudden Infant Death from the curated CTD Gene-Disease Associations dataset.

Death, Sudden, Cardiac Gene Set

From dbGAP Gene-Trait Associations

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

sudden infant death syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

myocardial infarct; cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; death, sudden; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden, cardiac; tachycardia, ventricular; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; brugada syndrome; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome; syncope; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sids/sudden infant death syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sids/sudden infant death syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart disease, ischemic; myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac death; cardiac morbidity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac death; cardiac morbidity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; depression; cardiac death; heart failure; angina; arrhythmia, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac death Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden infant death Gene Set

From GAD Gene-Disease Associations

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

death, sudden Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; sudden infant death Gene Set

From GAD Gene-Disease Associations

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

coronary artery disease; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden cardiac death Gene Set

From GAD Gene-Disease Associations

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

birth weight; sudden infant death Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; death Gene Set

From GAD Gene-Disease Associations

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

anemia; brain death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; brain death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; death, sudden, cardiac in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiac arrhythmias and sudden death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiac arrhythmias and sudden death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; death, sudden; heart septal defects, atrial; isolated noncompaction of the ventricular myocardium; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

staphylococcal infections; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease staphylococcal infections; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; heart diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; heart diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

sudden infant death syndrome (sids) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sudden infant death syndrome (sids) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadaver; cardiovascular diseases; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadaver; cardiovascular diseases; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset of sudden infant death. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of sudden infant death. 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.

death, sudden; pulmonary embolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular death Gene Set

From GAD Gene-Disease Associations

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

atrioventricular block; death, sudden; syncope; torsades de pointes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrioventricular block; death, sudden; syncope; torsades de pointes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; sudden infant death Gene Set

From GAD Gene-Disease Associations

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

coronary disease; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; death, sudden, cardiac; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long qt syndrome; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease long qt syndrome; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac 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.

anoxia; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

death, sudden, cardiac; long qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease death, sudden, cardiac; long qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; death, sudden, cardiac; myocardial infarction 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.

arrhythmias, cardiac; death, sudden, cardiac; Gene Set

From GAD Gene-Disease Associations

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

lipid metabolism, inborn errors; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipid metabolism, inborn errors; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ischemic neuronal cell death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ischemic neuronal cell death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; death, sudden; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sudden infant death syndrome Gene Set

From GAD Gene-Disease Associations

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

death Gene Set

From GeneRIF Biological Term Annotations

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

regulation of death-inducing signaling complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations dataset.

regulation of programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations dataset.

negative regulation of programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

death-inducing signaling complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations dataset.

negative regulation of neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of neuron death biological process from the curated GO Biological Process Annotations dataset.

mitochondrial outer membrane permeabilization involved in programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial outer membrane permeabilization involved in programmed cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-mediated programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

programmed necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the programmed necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

extrinsic apoptotic signaling pathway via death domain receptors Gene Set

From GO Biological Process Annotations

genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations dataset.

positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

modulation of programmed cell death in other organism Gene Set

From GO Biological Process Annotations

genes participating in the modulation of programmed cell death in other organism biological process from the curated GO Biological Process Annotations dataset.

positive regulation of hydrogen peroxide-mediated programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations dataset.

neuron death Gene Set

From GO Biological Process Annotations

genes participating in the neuron death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

developmental programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the developmental programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

death Gene Set

From GO Biological Process Annotations

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

positive regulation of neuron death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of neuron death biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-mediated programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations dataset.

necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

ectopic germ cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the ectopic germ cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation by symbiont of host programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cell death Gene Set

From GO Biological Process Annotations

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

positive regulation of activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

cell death Gene Set

From GO Biological Process Annotations

genes participating in the cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation by organism of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

regulation of cell death Gene Set

From GO Biological Process Annotations

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

positive regulation of cell death Gene Set

From GO Biological Process Annotations

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

negative regulation of hydrogen peroxide-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

modulation by symbiont of host programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the modulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

regulation of neuron death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of neuron death biological process from the curated GO Biological Process Annotations dataset.

regulation of hydrogen peroxide-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations dataset.

modulation of programmed cell death in other organism involved in symbiotic interaction Gene Set

From GO Biological Process Annotations

genes participating in the modulation of programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations dataset.

induction of programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the induction of programmed cell death biological process from the curated GO Biological Process Annotations dataset.

retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

host programmed cell death induced by symbiont Gene Set

From GO Biological Process Annotations

genes participating in the host programmed cell death induced by symbiont biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of death-inducing signaling complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of death-inducing signaling complex assembly biological process from the curated GO Biological Process Annotations dataset.

autophagic cell death Gene Set

From GO Biological Process Annotations

genes participating in the autophagic cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of mitochondrial membrane permeability involved in programmed necrotic cell death Gene Set

From GO Biological Process Annotations

genes participating in the regulation of mitochondrial membrane permeability involved in programmed necrotic cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene Set

From GO Biological Process Annotations

genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations dataset.

negative regulation by symbiont of host programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation by symbiont of host programmed cell death biological process from the curated GO Biological Process Annotations dataset.

programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the programmed cell death biological process from the curated GO Biological Process Annotations dataset.

death-inducing signaling complex Gene Set

From GO Cellular Component Annotations

proteins localized to the death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations dataset.

cd95 death-inducing signaling complex Gene Set

From GO Cellular Component Annotations

proteins localized to the cd95 death-inducing signaling complex cellular component from the curated GO Cellular Component Annotations dataset.

death receptor activity Gene Set

From GO Molecular Function Annotations

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

death effector domain binding Gene Set

From GO Molecular Function Annotations

genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations dataset.

death domain binding Gene Set

From GO Molecular Function Annotations

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

death receptor binding Gene Set

From GO Molecular Function Annotations

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

Aging (time to death) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Aging (time to death) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

sudden cardiac death Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sudden cardiac death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

time of death Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the time of death phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

sudden death Gene Set

From GWASdb SNP-Phenotype Associations

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

sudden cardiac death Gene Set

From HPO Gene-Disease Associations

genes associated with the sudden cardiac death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neonatal death Gene Set

From HPO Gene-Disease Associations

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

death in childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the death in childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

death in infancy Gene Set

From HPO Gene-Disease Associations

genes associated with the death in infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

time of death Gene Set

From HPO Gene-Disease Associations

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

sudden death Gene Set

From HPO Gene-Disease Associations

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

death in early adulthood Gene Set

From HPO Gene-Disease Associations

genes associated with the death in early adulthood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Brain Death Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Death Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Death, Sudden, Cardiac Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Death, Sudden Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Sudden Infant Death Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Death-like domain of Spt6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-like domain of Spt6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Domain of unknown function DUF2428, death-receptor-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Domain of unknown function DUF2428, death-receptor-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cell death regulator Aven Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cell death regulator Aven protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death-associated protein kinase 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death-associated protein kinase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

BH3-interacting domain death agonist Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the BH3-interacting domain death agonist protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Death effector domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Death effector domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Caffeine-induced death protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Caffeine-induced death protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Programmed cell death protein 2, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Programmed cell death protein 2, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal interdigital cell death Gene Set

From MPO Gene-Phenotype Associations

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

decreased sensitivity to induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sensitivity to induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal induced cell death Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cell death Gene Set

From MPO Gene-Phenotype Associations

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

decreased activation-induced cell death of t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cell death Gene Set

From MPO Gene-Phenotype Associations

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

premature death Gene Set

From MPO Gene-Phenotype Associations

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

pregnancy-related premature death Gene Set

From MPO Gene-Phenotype Associations

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

abnormal activation-induced cell death of t cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal activation-induced cell death of t cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cell death Gene Set

From MPO Gene-Phenotype Associations

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

{sudden infant death syndrome, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {sudden infant death syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

sudden infant death with dysgenesis of the testes syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the sudden infant death with dysgenesis of the testes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

death Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Cell death signalling via NRAGE, NRIF and NADE Gene Set

From Reactome Pathways

proteins participating in the Cell death signalling via NRAGE, NRIF and NADE pathway from the Reactome Pathways dataset.

Stimulation of the cell death response by PAK-2p34 Gene Set

From Reactome Pathways

proteins participating in the Stimulation of the cell death response by PAK-2p34 pathway from the Reactome Pathways dataset.

Death Receptor Signalling Gene Set

From Reactome Pathways

proteins participating in the Death Receptor Signalling pathway from the Reactome Pathways dataset.

TRIF-mediated programmed cell death Gene Set

From Reactome Pathways

proteins participating in the TRIF-mediated programmed cell death pathway from the Reactome Pathways dataset.

NADE modulates death signalling Gene Set

From Reactome Pathways

proteins participating in the NADE modulates death signalling pathway from the Reactome Pathways dataset.

NRIF signals cell death from the nucleus Gene Set

From Reactome Pathways

proteins participating in the NRIF signals cell death from the nucleus pathway from the Reactome Pathways dataset.

NRAGE signals death through JNK Gene Set

From Reactome Pathways

proteins participating in the NRAGE signals death through JNK pathway from the Reactome Pathways dataset.

Programmed Cell Death Gene Set

From Reactome Pathways

proteins participating in the Programmed Cell Death pathway from the Reactome Pathways 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 Weight Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fetal Weight 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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 Assocation 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.

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.

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.

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.

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 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.

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.

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 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.

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.

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.

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.

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.

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 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.

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 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.

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.

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.

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 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

genes participating in the fetal process involved in parturition biological process from the curated GO Biological Process Annotations 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 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 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.

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.

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 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.

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.

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.

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.

X-linked mental retardation 58 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 58 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, X-linked 45 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked mental retardation, syndromic, Claes-Jensen type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic, Claes-Jensen type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 63 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 63 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, X-linked, syndromic, turner type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, turner type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 30 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

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

Hypoparathyroidism retardation dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypoparathyroidism retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked mental retardation 90 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-Linked mental retardation 90 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked syndromic 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked syndromic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 29 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Syndromic X-linked mental retardation 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndromic X-linked mental retardation 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Siderius X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with marfanoid habitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wilson-Turner X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wilson-Turner X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, raymond type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, raymond type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, syndromic 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Birk Barel mental retardation dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Birk Barel mental retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ZNF711-Related X-linked Mental Retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ZNF711-Related X-linked Mental Retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 39 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Focal epilepsy with speech disorder with or without mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 38 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 38 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 34 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 34 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic 32 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic 32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, wu type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, wu type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked Mental Retardation 41 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-Linked Mental Retardation 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, Hedera type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, Hedera type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked syndromic mental retardation, Nascimento type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked syndromic mental retardation, Nascimento type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia, cerebellar ataxia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 47 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 47 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alacrima, achalasia, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 30 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

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

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 40 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 40 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 41 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 42 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 42 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 43 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 43 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 44 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 44 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 45 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 46 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 46 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 93 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 93 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 96 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 96 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 98 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 98 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 99 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 99 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 72 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 72 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Siderius X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Siderius X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.

Partington X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Partington X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.

Alopecia-Mental Retardation Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia-Mental Retardation Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Alopecia-Mental Retardation Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia-Mental Retardation Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 30 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 30 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 13 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 23 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 91 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 91 from the curated CTD Gene-Disease Associations dataset.

Miles-Carpenter x-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miles-Carpenter x-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 95 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 95 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 9 from the curated CTD Gene-Disease Associations dataset.

Hypoparathyroidism-retardation-dysmorphism syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoparathyroidism-retardation-dysmorphism syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 77 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 77 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 13 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 12 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 14 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.

Lubs X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lubs X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Fra12a Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Fra12a Type from the curated CTD Gene-Disease Associations dataset.

HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Short Stature Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Short Stature from the curated CTD Gene-Disease Associations dataset.

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 20 from the curated CTD Gene-Disease Associations dataset.

Mental retardation X-linked syndromic 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation X-linked syndromic 7 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Dominant 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Dominant 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 5 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Dominant 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 4 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 17 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Jarid1c-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Jarid1c-Related from the curated CTD Gene-Disease Associations dataset.

X-linked mental retardation Gustavson type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-linked mental retardation Gustavson type from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Female-Restricted, with Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Female-Restricted, with Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 81 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 81 from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked 14 from the curated CTD Gene-Disease Associations dataset.

Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type from the curated CTD Gene-Disease Associations dataset.

Mental retardation-hypotonic facies syndrome, x-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation-hypotonic facies syndrome, x-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Christianson Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Christianson Type from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 84 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 84 from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, syndromic 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, syndromic 5 from the curated CTD Gene-Disease Associations dataset.

BRACHYDACTYLY-MENTAL RETARDATION SYNDROME Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BRACHYDACTYLY-MENTAL RETARDATION SYNDROME from the curated CTD Gene-Disease Associations dataset.

Birk-Barel Mental Retardation Dysmorphism Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Birk-Barel Mental Retardation Dysmorphism Syndrome from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.

MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 21 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 21 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Epilepsy from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 9 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 78 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 78 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 73 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 73 from the curated CTD Gene-Disease Associations dataset.

Abidi X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abidi X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 4 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 82 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 82 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 11 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 10 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 96 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 96 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 8 from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 7 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 6 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 49 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 49 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Panhypopituitarism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Panhypopituitarism from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 52 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 52 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 53 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 53 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 58 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 58 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 from the curated CTD Gene-Disease Associations dataset.

PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 63 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 63 from the curated CTD Gene-Disease Associations dataset.

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset.

Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.

Armfield X-Linked Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Armfield X-Linked Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 42 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 42 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 93 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 93 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 94 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 94 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

Cleft Palate, Isolated, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cleft Palate, Isolated, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Turner Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Turner Type from the curated CTD Gene-Disease Associations dataset.

Microcephaly with Mental Retardation and Digital Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly with Mental Retardation and Digital Anomalies from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 72 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 72 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 45 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 45 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 46 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 46 from the curated CTD Gene-Disease Associations dataset.

Prieto X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prieto X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 10 from the curated CTD Gene-Disease Associations dataset.

Martin-Probst Deafness-Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Martin-Probst Deafness-Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 50 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 50 from the curated CTD Gene-Disease Associations dataset.

Cubitus Valgus with Mental Retardation and Unusual Facies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cubitus Valgus with Mental Retardation and Unusual Facies from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.

Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset.

Parkinsonism, early onset with mental retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinsonism, early onset with mental retardation from the curated CTD Gene-Disease Associations dataset.

non-specific x-linked mental retardation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease non-specific x-linked mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

epilepsy; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; rett syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

language development disorders; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease language development disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x syndrome; mental retardation; spinocerebellar degenerations; tremor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x syndrome; mental retardation; spinocerebellar degenerations; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x syndrome; fragile x syndromes; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x syndrome; fragile x syndromes; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

violent offenders with mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease violent offenders with mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukomalacia, periventricular; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukomalacia, periventricular; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

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

non-syndromic x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-syndromic x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epilepsy and mental retardation Gene Set

From GAD Gene-Disease Associations

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

brain diseases; mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain diseases; mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital abnormalities; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital abnormalities; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

learning disorders; memory disorders; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease learning disorders; memory disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation, x-linked; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation, x-linked; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; microcephaly Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; microcephaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation Gene Set

From GAD Gene-Disease Associations

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

retardation Gene Set

From GeneRIF Biological Term Annotations

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

Mental Retardation, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mental Retardation, X-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Mental Retardation Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Nuclear fragile X mental retardation-interacting protein 1, conserved domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nuclear fragile X mental retardation-interacting protein 1, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fragile X mental retardation protein family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fragile X mental retardation protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

mental retardation, severe, with spasticity and tapetoretinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, severe, with spasticity and tapetoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 9/26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 9/26 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 84 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 84 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 81 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 81 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 82 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 82 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 89 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 89 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 28 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 29 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 29 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation with language impairment and autistic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation with language impairment and autistic features phenotype from the curated OMIM Gene-Disease Associations dataset.

?rolandic epilepsy, mental retardation, and speech dyspraxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?rolandic epilepsy, mental retardation, and speech dyspraxia phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, snyder-robinson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, snyder-robinson type phenotype from the curated OMIM Gene-Disease Associations dataset.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 30/47 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 30/47 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked syndromic 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked syndromic 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, siderius type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, siderius type phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-thalassemia/mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-thalassemia/mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 40 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 40 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 44 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 44 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, fraxe type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, fraxe type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, armfield type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, armfield type phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked, syndromic 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From OMIM Gene-Disease Associations

genes associated with the psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated OMIM Gene-Disease Associations dataset.

corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.

alacrima, achalasia, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alacrima, achalasia, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

?arthrogryposis, mental retardation, and seizures Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?arthrogryposis, mental retardation, and seizures phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked, syndromic, hedera type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic, hedera type phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 91 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 91 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 90 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 90 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 98 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 98 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, shashi type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, shashi type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation-hypotonic facies syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation-hypotonic facies syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal dominant 22 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal dominant 22 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 78 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 78 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 72 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 72 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 52 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 52 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 53 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 53 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 50 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 50 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 58 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 58 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, claes-jensen type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic, claes-jensen type phenotype from the curated OMIM Gene-Disease Associations dataset.

waisman parkinsonism-mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the waisman parkinsonism-mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, nascimento-type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, nascimento-type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 21/34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 21/34 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 31 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 31 phenotype from the curated OMIM Gene-Disease Associations dataset.

?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

choroideremia, deafness, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the choroideremia, deafness, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 10/20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 10/20 phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?stocco dos santos x-linked mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?stocco dos santos x-linked mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

birk-barel mental retardation dysmorphism syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the birk-barel mental retardation dysmorphism syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 77 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 77 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 15 (cabezas type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 15 (cabezas type) phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

brachydactyly-mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the brachydactyly-mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with short stature Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with short stature phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive 43 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 43 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, chudley-schwartz type, Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic, chudley-schwartz type, phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 92 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 92 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 93 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 93 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 96 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 96 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 97 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 97 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 94 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 94 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 95 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 95 phenotype from the curated OMIM Gene-Disease Associations dataset.