Name

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.

alpha thalassemia; alpha-thalassemia; beta thalassemia; beta-thalassemia Gene Set

From GAD Gene-Disease Associations

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

alpha thalassemia; alpha-thalassemia; beta thalassemia; beta-thalassemia; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; beta thalassemia; beta-thalassemia; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia/mental retardation syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-thalassemia/mental retardation syndrome, type 1 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.

beta thalassemia; beta-thalassemia; bone diseases, metabolic; osteoporosis; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; bone diseases, metabolic; osteoporosis; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia; malaria, cerebral; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; elliptocytosis, hereditary; malaria, falciparum Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; elliptocytosis, hereditary; malaria, falciparum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; hydrops fetalis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; hydrops fetalis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia 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.

alpha thalassemia; alpha-thalassemia Gene Set

From GAD Gene-Disease Associations

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

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; bone necrosis; osteonecrosis; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, hypochromic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, hypochromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha thalassemia; alpha-thalassemia; anemia, sickle cell; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; beta-thalassemia; hiv infections; pregnancy complications, hematologic; pregnancy complications, infectious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; beta-thalassemia Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; overweight Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; sickle cell anemia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thalassemia; thalassemia, beta Gene Set

From GAD Gene-Disease Associations

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

beta thalassemia; beta-thalassemia; heterozygous haemoglobin s; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; heterozygous haemoglobin s; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; hemochromatosis; iron overload; metal metabolism, inborn errors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; hemochromatosis; iron overload; metal metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; hemochromatosis Gene Set

From GAD Gene-Disease Associations

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

anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; cardiomyopathies; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; cardiomyopathies; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; glucosephosphate dehydrogenase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; graft vs host disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; graft vs host disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; osteoporosis Gene Set

From GAD Gene-Disease Associations

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

beta thalassemia; beta-thalassemia; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; iron overload 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.

beta thalassemia; beta-thalassemia; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; hepatic veno-occlusive disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; hepatic veno-occlusive disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; hemoglobin sc disease; heterozygous haemoglobin s; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; hemoglobin sc disease; heterozygous haemoglobin s; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease 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.

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.

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.

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.

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.

Alpha-Thalassemia Myelodysplasia Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha-Thalassemia Myelodysplasia Syndrome from the curated CTD Gene-Disease Associations dataset.

alpha-thalassemia myelodysplasia syndrome, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-thalassemia myelodysplasia syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

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

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.

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.

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.

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.

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.

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, 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.

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.

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.

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.

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, 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.

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.

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.

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.

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.

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.

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.

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, 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.

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, 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 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.

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, 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.

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, 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.

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 syndromic, raymond type Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked syndromic, abidi type Gene Set

From OMIM Gene-Disease Associations

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

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, turner type Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked syndromic, lubs type Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, fra12a type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, fra12a type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, christianson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, christianson type phenotype from the curated OMIM Gene-Disease 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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-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.

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.

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.

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.

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.

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.

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.

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; 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.

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; 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.

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.

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.

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.

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.

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.

?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.

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.

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.

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.

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.

alopecia-mental retardation syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia-mental retardation syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia-mental retardation syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia-mental retardation syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia-mental retardation syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia-mental retardation syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?hyperphosphatasia with mental retardation syndrome 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis phenotype from the curated OMIM 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; 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.

Alpha trait thalassemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha trait thalassemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

alpha Thalassemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the alpha Thalassemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

alpha-Thalassemia Gene Set

From CTD Gene-Disease Associations

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

alpha thalassemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

alpha thalassemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, sickle cell; glucosephosphate dehydrogenase deficiency; hemolysis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; malaria; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; malaria; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia; malaria Gene Set

From GAD Gene-Disease Associations

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

alpha-thalassemia; anemia, sickle cell; cholelithiasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, sickle cell; cholelithiasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia Gene Set

From GAD Gene-Disease Associations

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

alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia, hypochromic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia, hypochromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thalassemia, alpha Gene Set

From GAD Gene-Disease Associations

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

alpha-Thalassemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

thalassemia, alpha- Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia, alpha- phenotype from the curated OMIM Gene-Disease Associations dataset.

4,6-Dideoxy-4-{[4,5,6-Trihydroxy-3-(Hydroxymethyl)Cyclohex-2-En-1-Yl]Amino}-Alpha-D-Lyxo-Hexopyranosyl-(1->4)-Alpha-D-Threo-Hexopyranosyl-(1->6)-Alpha-L-Threo-Hexopyranose Gene Set

From DrugBank Drug Targets

interacting proteins for the 4,6-Dideoxy-4-{[4,5,6-Trihydroxy-3-(Hydroxymethyl)Cyclohex-2-En-1-Yl]Amino}-Alpha-D-Lyxo-Hexopyranosyl-(1->4)-Alpha-D-Threo-Hexopyranosyl-(1->6)-Alpha-L-Threo-Hexopyranose drug from the curated DrugBank Drug Targets dataset.

5β-cholestane-3α 7α 12α-triol Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the 5β-cholestane-3α 7α 12α-triol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Alpha-D-phosphohexomutase, alpha/beta/alpha domain III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-D-phosphohexomutase, alpha/beta/alpha domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha-D-phosphohexomutase, alpha/beta/alpha domain I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-D-phosphohexomutase, alpha/beta/alpha domain I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha-D-phosphohexomutase, alpha/beta/alpha domain II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-D-phosphohexomutase, alpha/beta/alpha domain II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha-D-phosphohexomutase, alpha/beta/alpha I/II/III Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-D-phosphohexomutase, alpha/beta/alpha I/II/III protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chromosome 2q32-q33 deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromosome 2q32-q33 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

22q133 deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 22q133 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chromosome 1q43-q44 deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromosome 1q43-q44 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chromosome Xq28 deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromosome Xq28 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chromosome 9q deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromosome 9q deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homozygous 11p15-p14 Deletion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homozygous 11p15-p14 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

Jacobsen Distal 11q Deletion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Jacobsen Distal 11q Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

Chromosome 2q37 deletion syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chromosome 2q37 deletion syndrome from the curated CTD Gene-Disease Associations dataset.

22q11 Deletion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 22q11 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

Chromosome Xp11.3 Deletion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chromosome Xp11.3 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

Contiguous Abcd1/Dxs1375e Deletion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Contiguous Abcd1/Dxs1375e Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; digeorge syndrome Gene Set

From GAD Gene-Disease Associations

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

22q11 Deletion Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the 22q11 Deletion Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 7q11.23 deletion syndrome, distal, 1.2mb phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 4q21 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 4q21 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 6pter-p24 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 6pter-p24 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q26-qter deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q26-qter deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q12 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q12 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 18p deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 18p deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 2p16.1-p15 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 2p16.1-p15 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 2p12-p11.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 2p12-p11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1p36 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1p36 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 6q25-q25 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 6q25-q25 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q11.2 deletion syndrome, 1.4mb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q11.2 deletion syndrome, 1.4mb phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q25 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q25 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1p32-p31 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1p32-p31 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 22q11.2 deletion syndrome, distal Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 22q11.2 deletion syndrome, distal phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p11.2 deletion syndrome, 593kb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p11.2 deletion syndrome, 593kb phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p11.2 deletion syndrome, 220kb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p11.2 deletion syndrome, 220kb phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 11p15-p14 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 11p15-p14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

otodental dysplasia chromsome deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the otodental dysplasia chromsome deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p12.2-p11.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p12.2-p11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome xp11.3 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome xp11.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16q22 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16q22 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 18q deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 18q deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 8q21.11 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 8q21.11 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p13.3 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p13.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1q43-q44 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1q43-q44 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 13q14 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 13q14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 2q31.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 2q31.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 6q11-q14 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 6q11-q14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1q21.1 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1q21.1 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q11.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 3q13.31 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 3q13.31 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 9p deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 9p deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome xp21 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome xp21 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1q41-q42 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1q41-q42 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 10q26 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 10q26 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q24 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q24 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 19p13.13 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 19p13.13 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q23.1-q23.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q23.1-q23.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 19q13.11 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 19q13.11 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 14q11-q22 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 14q11-q22 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17p13.1 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17p13.1 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 5q14.3 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 5q14.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Beta-thalassemia, dominant inclusion body type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Beta-thalassemia, dominant inclusion body type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Beta Thalassemia, Dominant Inclusion Body Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Beta Thalassemia, Dominant Inclusion Body Type from the curated CTD Gene-Disease Associations 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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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, 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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, 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, 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.

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.

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.

?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 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, 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 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.

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.

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.

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.

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.

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

From OMIM Gene-Disease Associations

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

mental retardation, 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 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.

mental retardation, x-linked 99 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 99 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 39 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 39 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 38 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 38 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 31 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 31 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 33 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 33 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 35 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 35 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 34 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 36 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 36 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

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

scaphocephaly, maxillary retrusion, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the scaphocephaly, maxillary retrusion, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 23 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 24 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 26 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 29 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation-skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation-skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 13 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 12 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 16 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 15 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 14 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 19 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 18 Gene Set

From OMIM Gene-Disease Associations

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

cubitus valgus with mental retardation and unusual facies Gene Set

From OMIM Gene-Disease Associations

genes associated with the cubitus valgus with mental retardation and unusual facies phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia, nonprogressive, with mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia, nonprogressive, with mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, with or without nystagmus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 63 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 63 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 101 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 101 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 100 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 100 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 49 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 49 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, focal, with speech disorder and with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal dominant 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal dominant 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 23 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 29 and others Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 29 and others phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant, 27 Gene Set

From OMIM Gene-Disease Associations

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

megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive, 37 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive, 37 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant, 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant, 28 phenotype from the curated OMIM 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.

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; 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.

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.

birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal 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.

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

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal 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 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.

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.

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.

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.

sickle cell anemia; thalassemia; gilbert syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sickle cell anemia; thalassemia; gilbert syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Chromosome 17 deletion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chromosome 17 deletion from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, Associated With Chromosome 5q Deletion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, Associated With Chromosome 5q Deletion from the curated CTD Gene-Disease Associations dataset.

adenocarcinoma; chromosome deletion; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; chromosome deletion; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; chromosome deletion; head and neck neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; chromosome deletion; head and neck neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

chromosome deletion; infertility, male Gene Set

From GAD Gene-Disease Associations

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

chromosome deletion Gene Set

From GAD Gene-Disease Associations

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

brill-symmers disease; chromosome deletion; lymphoma, follicular Gene Set

From GAD Gene-Disease Associations

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

chromosome deletion; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

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

adenocarcinoma; biliary tract neoplasm; biliary tract neoplasms; chromosome deletion; diabetes complications; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; biliary tract neoplasm; biliary tract neoplasms; chromosome deletion; diabetes complications; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; epilepsy, generalized; Gene Set

From GAD Gene-Disease Associations

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

altitude sickness; chromosome deletion; pulmonary edema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease altitude sickness; chromosome deletion; pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; chromosome deletion Gene Set

From GAD Gene-Disease Associations

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

deletion-insertion and alternative splicing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deletion-insertion and alternative splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome deletion; dystonia; myoclonus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome deletion; dystonia; myoclonus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

full-length deletion of the tyrosinase gene Gene Set

From GAD Gene-Disease Associations

genes associated with the disease full-length deletion of the tyrosinase gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene Set

From GAD Gene-Disease Associations

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

c4gene deletion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease c4gene deletion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome deletion; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deletion Gene Set

From GeneRIF Biological Term Annotations

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

dna insertion or deletion binding Gene Set

From GO Molecular Function Annotations

genes performing the dna insertion or deletion binding molecular function from the curated GO Molecular Function Annotations dataset.

dinucleotide insertion or deletion binding Gene Set

From GO Molecular Function Annotations

genes performing the dinucleotide insertion or deletion binding molecular function from the curated GO Molecular Function Annotations dataset.

single base insertion or deletion binding Gene Set

From GO Molecular Function Annotations

genes performing the single base insertion or deletion binding molecular function from the curated GO Molecular Function Annotations dataset.

Chromosome Deletion Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal clonal deletion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal t cell clonal deletion Gene Set

From MPO Gene-Phenotype Associations

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

macrocytic anemia, refractory, due to 5q deletion, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocytic anemia, refractory, due to 5q deletion, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 5q12 deletion sydrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 5q12 deletion sydrome phenotype from the curated OMIM Gene-Disease Associations dataset.

sequence-deletion Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Beta thalassemia major Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Beta thalassemia major phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Beta thalassemia intermedia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Beta thalassemia intermedia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Delta-0-thalassemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Delta-0-thalassemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

delta Thalassemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the delta Thalassemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

beta Thalassemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the beta Thalassemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

beta^0^ Thalassemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the beta^0^ Thalassemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

beta-Thalassemia Gene Set

From CTD Gene-Disease Associations

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

beta thalassemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

thalassemia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

thalassemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

thalassemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

beta thalassemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

thalassemia Gene Set

From GAD Gene-Disease Associations

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

beta-thalassemia major Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; sickle cell anemia; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; sickle cell anemia; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholelithiasis; thalassemia Gene Set

From GAD Gene-Disease Associations

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

beta-thalassemia; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta-thalassemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemoglobinopathies; thalassemia Gene Set

From GAD Gene-Disease Associations

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

hemochromatosis; thalassemia Gene Set

From GAD Gene-Disease Associations

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

beta-thalassemia; cholelithiasis Gene Set

From GAD Gene-Disease Associations

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

beta thalassemia Gene Set

From GAD Gene-Disease Associations

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

dyslipidemias; thalassemia Gene Set

From GAD Gene-Disease Associations

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

beta thalassemia/hemoglobin e disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia/hemoglobin e disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome inversion; hemochromatosis; inversion, chromosome; iron overload; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome inversion; hemochromatosis; inversion, chromosome; iron overload; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

iron overload; thalassemia Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; beta-thalassemia; hemoglobinopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta-thalassemia; hemoglobinopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta-thalassemia; osteoporosis Gene Set

From GAD Gene-Disease Associations

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

beta-thalassemia Gene Set

From GAD Gene-Disease Associations

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

beta-thalassemia; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

thalassemia, beta Gene Set

From GAD Gene-Disease Associations

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

anemia; hemoglobinopathies; iron overload; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; hemoglobinopathies; iron overload; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta(0)-thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta(0)-thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thalassemia Gene Set

From GeneRIF Biological Term Annotations

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

Beta thalassemia/hemoglobin E disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Beta thalassemia/hemoglobin E disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

beta thalassemia Gene Set

From GWASdb SNP-Disease Associations

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

thalassemia Gene Set

From GWASdb SNP-Disease Associations

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

beta-Thalassemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Thalassemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

thalassemia-beta, dominant inclusion-body Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia-beta, dominant inclusion-body phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia with beta-thalassemia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia with beta-thalassemia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

thalassemia, delta- Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia, delta- phenotype from the curated OMIM Gene-Disease Associations dataset.

delta-beta thalassemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the delta-beta thalassemia phenotype from the curated OMIM Gene-Disease Associations dataset.

thalassemia due to hb lepore Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia due to hb lepore phenotype from the curated OMIM Gene-Disease Associations dataset.

thalassemia, hispanic gamma-delta-beta Gene Set

From OMIM Gene-Disease Associations

genes associated with the thalassemia, hispanic gamma-delta-beta phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha,alpha-trehalose-phosphate synthase complex (udp-forming) Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the alpha,alpha-trehalose-phosphate synthase complex (udp-forming) cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

SIRT1-HNF4-alpha-PGC-1-alpha complex, in response to fasting Gene Set

From CORUM Protein Complexes

proteins in the SIRT1-HNF4-alpha-PGC-1-alpha complex, in response to fasting protein complex from the CORUM Protein Complexes dataset.

Casein kinase II (beta-dimer, alpha, alpha') Gene Set

From CORUM Protein Complexes

proteins in the Casein kinase II (beta-dimer, alpha, alpha') protein complex from the CORUM Protein Complexes dataset.

PCNA-MutS-alpha-MutL-alpha-DNA complex Gene Set

From CORUM Protein Complexes

proteins in the PCNA-MutS-alpha-MutL-alpha-DNA complex protein complex from the CORUM Protein Complexes dataset.

IKK-alpha--ER-alpha-AIB1 complex Gene Set

From CORUM Protein Complexes

proteins in the IKK-alpha--ER-alpha-AIB1 complex protein complex from the CORUM Protein Complexes dataset.

4,4'-(carbonylbis(imino-3,1-phenylenecarbonylimino-3,1-(4-methylphenylene)carbonylimino))bis(1,3-xylene-alpha,alpha'-diphosphonic acid) Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 4,4'-(carbonylbis(imino-3,1-phenylenecarbonylimino-3,1-(4-methylphenylene)carbonylimino))bis(1,3-xylene-alpha,alpha'-diphosphonic acid) from the curated CTD Gene-Chemical Interactions dataset.

2-(4-((dimethylamino)carbonyl)-3-fluorophenyl)-alpha,alpha-dimethyl-N-1,3,4-thiadiazol-2-yl-5H-(1)benzopyrano(2,3-b)pyridin-5-acetamide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 2-(4-((dimethylamino)carbonyl)-3-fluorophenyl)-alpha,alpha-dimethyl-N-1,3,4-thiadiazol-2-yl-5H-(1)benzopyrano(2,3-b)pyridin-5-acetamide from the curated CTD Gene-Chemical Interactions dataset.

6,6'-bis(2,3-dimethoxybenzoyl)-alpha,alpha-trehalose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 6,6'-bis(2,3-dimethoxybenzoyl)-alpha,alpha-trehalose from the curated CTD Gene-Chemical Interactions dataset.

15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid from the curated CTD Gene-Chemical Interactions dataset.

alpha,alpha-dimethoxytoluene Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical alpha,alpha-dimethoxytoluene from the curated CTD Gene-Chemical Interactions dataset.

5-2-(4-((ethylmethylamino)carbonyl)-3-fluorophenyl)-alpha,alpha-dimethyl-N-1,3,4-thiadiazol-2-yl-5H-(1)benzopyrano(2,3-b)pyridin-5-acetamide Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 5-2-(4-((ethylmethylamino)carbonyl)-3-fluorophenyl)-alpha,alpha-dimethyl-N-1,3,4-thiadiazol-2-yl-5H-(1)benzopyrano(2,3-b)pyridin-5-acetamide from the curated CTD Gene-Chemical Interactions dataset.

5-Alpha-Androstane-3-Beta,17-Alpha-Diol Gene Set

From DrugBank Drug Targets

interacting proteins for the 5-Alpha-Androstane-3-Beta,17-Alpha-Diol drug from the curated DrugBank Drug Targets dataset.

Methyl-2-S-(Alpha-D-Mannopyranosyl)-2-Thio-Alpha-D-Mannopyranoside Gene Set

From DrugBank Drug Targets

interacting proteins for the Methyl-2-S-(Alpha-D-Mannopyranosyl)-2-Thio-Alpha-D-Mannopyranoside drug from the curated DrugBank Drug Targets dataset.

alpha-n-acetylneuraminate alpha-2,8-sialyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the alpha-n-acetylneuraminate alpha-2,8-sialyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

alpha,alpha-trehalase activity Gene Set

From GO Molecular Function Annotations

genes performing the alpha,alpha-trehalase activity molecular function from the curated GO Molecular Function Annotations dataset.

(alpha-n-acetylneuraminyl-2,3-beta-galactosyl-1,3)-n-acetyl-galactosaminide 6-alpha-sialyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the (alpha-n-acetylneuraminyl-2,3-beta-galactosyl-1,3)-n-acetyl-galactosaminide 6-alpha-sialyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

17-alpha,20-alpha-dihydroxypregn-4-en-3-one dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the 17-alpha,20-alpha-dihydroxypregn-4-en-3-one dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

alpha-n-acetylgalactosaminide alpha-2,6-sialyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the alpha-n-acetylgalactosaminide alpha-2,6-sialyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

5α-pregnan-3α-ol-20-one Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the 5α-pregnan-3α-ol-20-one ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

(3α 5β 12α 17xi)-3-hydroxy-21-[(2R 4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl]pregnan-12-yl (2S)-2-methylbutanoate Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the (3α 5β 12α 17xi)-3-hydroxy-21-[(2R 4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl]pregnan-12-yl (2S)-2-methylbutanoate ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

3-alpha,20-alpha-Dihydroxy-5-beta-pregnane 3-glucuronide Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 3-alpha,20-alpha-Dihydroxy-5-beta-pregnane 3-glucuronide metabolite from the curated HMDB Metabolites of Enzymes dataset.

3 alpha,7 alpha,24-Trihydroxy-5beta-cholestanoyl-CoA Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 3 alpha,7 alpha,24-Trihydroxy-5beta-cholestanoyl-CoA metabolite from the curated HMDB Metabolites of Enzymes dataset.

D-Gal alpha 1->6D-Gal alpha 1->6D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the D-Gal alpha 1->6D-Gal alpha 1->6D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

4-alpha-Methyl-5-alpha-cholest-7-en-3-one Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4-alpha-Methyl-5-alpha-cholest-7-en-3-one metabolite from the curated HMDB Metabolites of Enzymes dataset.

4-beta-Hydroxymethyl-4-alpha-methyl-5-alpha-cholest-7-en-3-beta-ol Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4-beta-Hydroxymethyl-4-alpha-methyl-5-alpha-cholest-7-en-3-beta-ol metabolite from the curated HMDB Metabolites of Enzymes dataset.

3-beta-Hydroxy-4-beta-methyl-5-alpha-cholest-7-ene-4-alpha-carboxylate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 3-beta-Hydroxy-4-beta-methyl-5-alpha-cholest-7-ene-4-alpha-carboxylate metabolite from the curated HMDB Metabolites of Enzymes dataset.

4-alpha-Methyl-5-alpha-cholest-7-en-3-beta-ol Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4-alpha-Methyl-5-alpha-cholest-7-en-3-beta-ol metabolite from the curated HMDB Metabolites of Enzymes dataset.

3-alpha-hydroxy-5-alpha-androstane-17-one 3-D-glucuronide Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 3-alpha-hydroxy-5-alpha-androstane-17-one 3-D-glucuronide metabolite from the curated HMDB Metabolites of Enzymes dataset.

17-alpha,20-alpha-Dihydroxypregn-4-en-3-one Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 17-alpha,20-alpha-Dihydroxypregn-4-en-3-one metabolite from the curated HMDB Metabolites of Enzymes dataset.

3 alpha,7 alpha,26-Trihydroxy-5beta-cholestane Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 3 alpha,7 alpha,26-Trihydroxy-5beta-cholestane metabolite from the curated HMDB Metabolites of Enzymes dataset.

3-beta-Hydroxy-4-beta-methyl-5-alpha-cholest-7-ene-4-alpha-carbaldehyde Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 3-beta-Hydroxy-4-beta-methyl-5-alpha-cholest-7-ene-4-alpha-carbaldehyde metabolite from the curated HMDB Metabolites of Enzymes dataset.

Rossmann-like alpha/beta/alpha sandwich fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Rossmann-like alpha/beta/alpha sandwich fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mog1/PsbP, alpha/beta/alpha sandwich Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mog1/PsbP, alpha/beta/alpha sandwich protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha, subdomain 1/3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha, subdomain 1/3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Terpenoid cyclases/protein prenyltransferase alpha-alpha toroid Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Terpenoid cyclases/protein prenyltransferase alpha-alpha toroid protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aconitase/3-isopropylmalate dehydratase large subunit, alpha/beta/alpha, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alkaline phosphatase-like, alpha/beta/alpha Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alkaline phosphatase-like, alpha/beta/alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset.

BRD-K20168484_1h-indole-2-propanoic acid, 1-[(4-chlorophenyl)methyl]-3-[(1,1-dimethylethyl)thio]-alpha,alpha-dimethyl-5-(1-methylethyl)- [cas]_A549_24.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K20168484_1h-indole-2-propanoic acid, 1-[(4-chlorophenyl)methyl]-3-[(1,1-dimethylethyl)thio]-alpha,alpha-dimethyl-5-(1-methylethyl)- [cas]_A549_24.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

BRD-K20168484_1h-indole-2-propanoic acid, 1-[(4-chlorophenyl)methyl]-3-[(1,1-dimethylethyl)thio]-alpha,alpha-dimethyl-5-(1-methylethyl)- [cas]_PC3_24.0_h_10.0_um Gene Set

From LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the BRD-K20168484_1h-indole-2-propanoic acid, 1-[(4-chlorophenyl)methyl]-3-[(1,1-dimethylethyl)thio]-alpha,alpha-dimethyl-5-(1-methylethyl)- [cas]_PC3_24.0_h_10.0_um small molecule perturbation from the LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway Gene Set

From PANTHER Pathways

proteins participating in the Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway pathway from the PANTHER Pathways dataset.

Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway Gene Set

From PANTHER Pathways

proteins participating in the Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway pathway from the PANTHER Pathways dataset.

albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; chronic renal failure; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; glycosuria; kidney failure, chronic; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 1; diabetes mellitus, type 2; hypoglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic angiopathies; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; disease susceptibility; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; genetic predisposition to disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; hypertension; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic angiopathies; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Growth mental deficiency syndrome of Myhre Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth mental deficiency syndrome of Myhre from the curated CTD Gene-Disease 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.

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.

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.

hypoparathyroidism-retardation-dysmorphism syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoparathyroidism-retardation-dysmorphism syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; wolfram syndrome Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; insulin resistance; metabolic syndrome x; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; obesity Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus type ii; diabetes mellitus, type 2; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

Prolyl 4-hydroxylase (alpha(I)-type) Gene Set

From CORUM Protein Complexes

proteins in the Prolyl 4-hydroxylase (alpha(I)-type) protein complex from the CORUM Protein Complexes dataset.

Prolyl 4-hydroxylase (alpha(III)-type) Gene Set

From CORUM Protein Complexes

proteins in the Prolyl 4-hydroxylase (alpha(III)-type) protein complex from the CORUM Protein Complexes dataset.

Voltage-dependent calcium channel, T-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, T-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1C subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1C subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase I, catalytic core, alpha-helical subdomain, eukaryotic-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase I, catalytic core, alpha-helical subdomain, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha-(1,6)-fucosyltransferase, eukaryotic type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-(1,6)-fucosyltransferase, eukaryotic type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, T-type, alpha-1I subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, T-type, alpha-1I subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Receptor tyrosine-protein phosphatase, alpha/epsilon-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Receptor tyrosine-protein phosphatase, alpha/epsilon-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, N-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, N-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, R-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, R-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytochrome P450, cholesterol 7-alpha-monooxygenase-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytochrome P450, cholesterol 7-alpha-monooxygenase-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein kinase C, alpha/beta/gamma types Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein kinase C, alpha/beta/gamma types protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel,T-type, alpha-1G subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel,T-type, alpha-1G subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sterile alpha motif, type 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sterile alpha motif, type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sterile alpha motif, type 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sterile alpha motif, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Alpha-L-fucosidase, metazoa-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Alpha-L-fucosidase, metazoa-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase I, DNA binding, mixed alpha/beta motif, eukaryotic-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase I, DNA binding, mixed alpha/beta motif, eukaryotic-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Prefoldin alpha subunit, archaea-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Prefoldin alpha subunit, archaea-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1F subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1F subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1D subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1D subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, P/Q-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, P/Q-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

V-type ATP synthase catalytic alpha chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the V-type ATP synthase catalytic alpha chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, T-type, alpha-1H subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, T-type, alpha-1H subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IIA, subunit A/ C-terminal, alpha-beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IIA, subunit A/ C-terminal, alpha-beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1S subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1S subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Type IIA DNA topoisomerase subunit A, alpha-helical domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Type IIA DNA topoisomerase subunit A, alpha-helical domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

mannosidosis, alpha-, types i and ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the mannosidosis, alpha-, types i and ii phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha 1-antitrypsin deficiency; aortic stenosis, supravalvular; dislocations; scoliosis; williams syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Aniridia cerebellar ataxia mental deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aniridia cerebellar ataxia mental deficiency from the curated CTD Gene-Disease Associations dataset.

Mental Disorders Gene Set

From CTD Gene-Disease Associations

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

MENTAL HEALTH WELLNESS 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL HEALTH WELLNESS 1 from the curated CTD Gene-Disease Associations dataset.

Mental Disorders Diagnosed in Childhood Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Disorders Diagnosed in Childhood from the curated CTD Gene-Disease Associations dataset.

MENTAL HEALTH WELLNESS 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL HEALTH WELLNESS 2 from the curated CTD Gene-Disease Associations dataset.

Mental Disorders Gene Set

From dbGAP Gene-Trait Associations

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

Mental Competency Gene Set

From dbGAP Gene-Trait Associations

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

Mental Processes Gene Set

From dbGAP Gene-Trait Associations

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

developmental disorder of mental health Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease developmental disorder of mental health from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

disease of mental health Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease disease of mental health from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

mental depression Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

developmental disorder of mental health Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

disease of mental health Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease disease of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

mental depression Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alcohol-induced mental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

disease of mental health Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

developmental disorder of mental health Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

drug-induced mental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mental development Gene Set

From GAD Gene-Disease Associations

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

mental disorder Gene Set

From GAD Gene-Disease Associations

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

confusion; confusion (mental); dementia; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease confusion; confusion (mental); dementia; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental disorders Gene Set

From GAD Gene-Disease Associations

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

mental illness Gene Set

From GAD Gene-Disease Associations

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

mental processes Gene Set

From GAD Gene-Disease Associations

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

mental competency Gene Set

From GAD Gene-Disease Associations

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

mental Gene Set

From GeneRIF Biological Term Annotations

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

mental depression Gene Set

From GWASdb SNP-Disease Associations

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

drug-induced mental disorder Gene Set

From GWASdb SNP-Disease Associations

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

alcohol-induced mental disorder Gene Set

From GWASdb SNP-Disease Associations

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

developmental disorder of mental health Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease developmental disorder of mental health in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

disease of mental health Gene Set

From GWASdb SNP-Disease Associations

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

mental deterioration Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of higher mental function Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of higher mental function Gene Set

From HPO Gene-Disease Associations

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

mental deterioration Gene Set

From HPO Gene-Disease Associations

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

Mental Processes Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Competency Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Health Services Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Fatigue Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Health Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Community Mental Health Services Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Recall Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mental Status Schedule Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

MENTAL domain Gene Set

From InterPro Predicted Protein Domain Annotations

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

{mental health wellness-1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {mental health wellness-1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{mental health wellness-2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {mental health wellness-2} phenotype from the curated OMIM Gene-Disease 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.

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.

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.

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.

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.

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.

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.

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.

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.

abruptio placentae; fetal growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

fetal 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; hypertension; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy, left ventricular; left ventricular hypertrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hyperinsulinism; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary disease; coronary heart disease; familial type 3 hyperlipoproteinaemia; hyperinsulinism; hyperlipoproteinemia type iii; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hypertrophy; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; edema Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 2; hyperlipoproteinemia type i; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; hyperlipoproteinemia type i; hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

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

birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hemochromatosis; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic neuropathies; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

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

familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial type 3 hyperlipoproteinaemia; hyperlipoproteinemia type iii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hyperlipidemias; obesity Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension; obesity Gene Set

From GAD Gene-Disease Associations

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

deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes mellitus, type 1; diabetes mellitus, type 2; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy; diabetic neuropathies; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; chronic renal failure; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; kidney failure, chronic; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2 ; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2 ; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; diabetes mellitus type ii; diabetes mellitus, type 2; dyslipidemias Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; hypertension Gene Set

From GAD Gene-Disease Associations

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

colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; coronary disease; coronary heart disease; diabetes mellitus type ii; diabetes mellitus, type 2; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; endometrial neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

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

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute-phase reaction; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; diabetes complications; diabetes mellitus type ii; diabetes mellitus, type 2; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; diabetes mellitus type ii; diabetes mellitus, type 2; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; diabetes, gestational; gestational diabetes mellitus Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; diabetes mellitus type ii; diabetes mellitus, type 2; diabetic nephropathies; diabetic nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set

From GAD Gene-Disease Associations

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

arteriosclerosis; diabetes mellitus type ii; diabetes mellitus, type 2 Gene Set