Name

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.

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.

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.

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.

Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype 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 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.

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.

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.

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.

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 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 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 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.

schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety disorder; depressive disorder, major; panic disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety disorder; depressive disorder, major; panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit disorder; conduct disorder; oppositional defiant disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit disorder; conduct disorder; oppositional defiant disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

conduct disorder; oppositional defiant disorder; antisocial personality disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease conduct disorder; oppositional defiant disorder; antisocial personality disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; attention deficit disorder; conduct disorder; oppositional defiant disorder; dementia, frontotemporal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; attention deficit disorder; conduct disorder; oppositional defiant disorder; dementia, frontotemporal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pervasive developmental disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

specific developmental disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

specific developmental disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

pervasive developmental disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

pervasive developmental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

developmental coordination disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

specific developmental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

specific developmental disorder Gene Set

From GWASdb SNP-Disease Associations

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

pervasive developmental disorder Gene Set

From GWASdb SNP-Disease Associations

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

health perception Gene Set

From GAD Gene-Disease Associations

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

ill health, sheep dip related Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ill health, sheep dip related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

healthy oldest-old Gene Set

From GAD Gene-Disease Associations

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

healthrelated Gene Set

From GeneRIF Biological Term Annotations

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

healthy Gene Set

From GeneRIF Biological Term Annotations

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

healthier Gene Set

From GeneRIF Biological Term Annotations

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

health Gene Set

From GeneRIF Biological Term Annotations

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

healthrelevant Gene Set

From GeneRIF Biological Term Annotations

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

Self-rated health Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Self-rated health phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Foie gras liver health family 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Foie gras liver health family 1 protein domain from the InterPro Predicted Protein Domain Annotations 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.

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.

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 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.

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.

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.

bipolar disorder; affective disorder Gene Set

From GAD Gene-Disease Associations

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

depressive disorder, major; bipolar disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depressive disorder, major; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bipolar disorder; unipolar disorder Gene Set

From GAD Gene-Disease Associations

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

schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizoaffective disorder; alcoholism; bipolar disorder; suicide Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizoaffective disorder; alcoholism; bipolar disorder; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit hyperactivity disorder and conduct disorder Gene Set

From GAD Gene-Disease Associations

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

bipolar affective disorder; unipolar affective disorder Gene Set

From GAD Gene-Disease Associations

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

conduct disorder; hyperkinetic disorder Gene Set

From GAD Gene-Disease Associations

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

major depressive disorder and panic disorder Gene Set

From GAD Gene-Disease Associations

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

antisocial personality disorder attention deficit hyperactivity disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antisocial personality disorder attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; bipolar disorder; affective disorder Gene Set

From GAD Gene-Disease Associations

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

schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

seasonal affective disorder; premenstrual dysphoric disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease seasonal affective disorder; premenstrual dysphoric disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit disorder; seasonal affective disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit disorder; seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depressive disorder, major; bipolar disorder; affective psychoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depressive disorder, major; bipolar disorder; affective psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; schizoaffective disorder; bipolar disorder Gene Set

From GAD Gene-Disease Associations

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

depressive disorder, major; bipolar disorder; suicide Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depressive disorder, major; bipolar disorder; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; depressive disorder, major; bipolar disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; depressive disorder, major; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety disorder; depressive disorder, major; neuroticism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety disorder; depressive disorder, major; neuroticism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; schizoaffective disorder; affective disorder Gene Set

From GAD Gene-Disease Associations

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

attention deficit disorder; conduct disorder; aggressive behavior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit disorder; conduct disorder; aggressive behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Schizophrenia, schizoaffective disorder or bipolar disorder Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Schizophrenia, schizoaffective disorder or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Attention deficit hyperactivity disorder and conduct disorder Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Attention deficit hyperactivity disorder and conduct disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bipolar disorder and major depressive disorder (combined) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bipolar disorder and major depressive disorder (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-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.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Obesity, hyperphagia, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Obesity, hyperphagia, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

DEVELOPMENTAL DYSPLASIA OF THE HIP 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEVELOPMENTAL DYSPLASIA OF THE HIP 1 from the curated CTD Gene-Disease Associations dataset.

Developmental Disabilities Gene Set

From CTD Gene-Disease Associations

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

Bone Diseases, Developmental Gene Set

From CTD Gene-Disease Associations

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

MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay 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.

anodontia; developmental absence of tooth Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anodontia; developmental absence of tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, developmental; osteoarthritis, hip Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, developmental; osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

developmental Gene Set

From GAD High Level Gene-Disease Associations

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

developmental Gene Set

From GeneRIF Biological Term Annotations

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

developmental maturation Gene Set

From GO Biological Process Annotations

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

positive regulation of developmental growth Gene Set

From GO Biological Process Annotations

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

developmental programmed cell death Gene Set

From GO Biological Process Annotations

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

developmental growth involved in morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the developmental growth involved in morphogenesis biological process from the curated GO Biological Process Annotations dataset.

single-organism developmental process Gene Set

From GO Biological Process Annotations

genes participating in the single-organism developmental process biological process from the curated GO Biological Process Annotations dataset.

cellular developmental process Gene Set

From GO Biological Process Annotations

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

regulation of developmental pigmentation Gene Set

From GO Biological Process Annotations

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

negative regulation of developmental growth Gene Set

From GO Biological Process Annotations

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

negative regulation of developmental pigmentation Gene Set

From GO Biological Process Annotations

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

regulation of developmental process Gene Set

From GO Biological Process Annotations

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

developmental growth Gene Set

From GO Biological Process Annotations

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

developmental cell growth Gene Set

From GO Biological Process Annotations

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

negative regulation of developmental process Gene Set

From GO Biological Process Annotations

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

pigment metabolic process involved in developmental pigmentation Gene Set

From GO Biological Process Annotations

genes participating in the pigment metabolic process involved in developmental pigmentation biological process from the curated GO Biological Process Annotations dataset.

developmental induction Gene Set

From GO Biological Process Annotations

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

developmental process involved in reproduction Gene Set

From GO Biological Process Annotations

genes participating in the developmental process involved in reproduction biological process from the curated GO Biological Process Annotations dataset.

developmental pigmentation Gene Set

From GO Biological Process Annotations

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

positive regulation of developmental process Gene Set

From GO Biological Process Annotations

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

regulation of developmental growth Gene Set

From GO Biological Process Annotations

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

positive regulation of developmental pigmentation Gene Set

From GO Biological Process Annotations

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

developmental process Gene Set

From GO Biological Process Annotations

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

spongiotrophoblast layer developmental growth Gene Set

From GO Biological Process Annotations

genes participating in the spongiotrophoblast layer developmental growth biological process from the curated GO Biological Process Annotations dataset.

developmental stagnation Gene Set

From HPO Gene-Disease Associations

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

moderate global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the moderate global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

developmental stagnation at onset of seizures Gene Set

From HPO Gene-Disease Associations

genes associated with the developmental stagnation at onset of seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mild global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the mild global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

developmental regression Gene Set

From HPO Gene-Disease Associations

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

global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe global developmental delay Gene Set

From HPO Gene-Disease Associations

genes associated with the severe global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Developmental Disabilities Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Bone Diseases, Developmental Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Developmental pluripotency-associated protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Developmental pluripotency-associated protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Developmental pluripotency-associated protein 2/4, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Developmental pluripotency-associated protein 2/4, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sox developmental protein N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sox developmental protein N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Developmental pluripotency-associated protein 2/4, central domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Developmental pluripotency-associated protein 2/4, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Interferon-related developmental regulator, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Interferon-related developmental regulator, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Interferon-related developmental regulator, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Interferon-related developmental regulator, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal developmental patterning Gene Set

From MPO Gene-Phenotype Associations

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

abnormal developmental vascular remodeling Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal developmental vascular remodeling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

developmental dysplasia of the hip 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the developmental dysplasia of the hip 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, hyperphagia, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, hyperphagia, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, seizures, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, seizures, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

?obesity, hyperphagia, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?obesity, hyperphagia, and developmental delay 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.

sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

developmental Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Developmental Biology Gene Set

From Reactome Pathways

proteins participating in the Developmental Biology pathway from the Reactome Pathways dataset.

X-linked mental retardation 58 Gene Set

From ClinVar Gene-Phenotype Associations

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

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, X-linked 45 Gene Set

From ClinVar Gene-Phenotype Associations

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

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

X-linked mental retardation 63 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 7 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 5 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

X-linked mental retardation 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 30 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 24 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 28 Gene Set

From ClinVar Gene-Phenotype Associations

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

X-Linked mental retardation 90 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation X-linked syndromic 5 Gene Set

From ClinVar Gene-Phenotype Associations

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

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 23 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 27 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 29 Gene Set

From ClinVar Gene-Phenotype Associations

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

Syndromic X-linked mental retardation 16 Gene Set

From ClinVar Gene-Phenotype Associations

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

Siderius X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked mental retardation with marfanoid habitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Wilson-Turner X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked mental retardation 18 Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

X-linked mental retardation, syndromic 14 Gene Set

From ClinVar Gene-Phenotype Associations

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

Birk Barel mental retardation dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperphosphatasia with mental retardation syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperphosphatasia with mental retardation syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperphosphatasia with mental retardation syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperphosphatasia with mental retardation syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

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

Hyperphosphatasia with mental retardation syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation, X-linked 19 Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 9 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal dominant 8 Gene Set

From ClinVar Gene-Phenotype Associations

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

ZNF711-Related X-linked Mental Retardation Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 18 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 27 Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 39 Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

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

From ClinVar Gene-Phenotype Associations

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

X-Linked Mental Retardation 41 Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 13 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 12 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 14 Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked syndromic mental retardation, Nascimento type Gene Set

From ClinVar Gene-Phenotype Associations

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

Aniridia, cerebellar ataxia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Mental retardation, autosomal recessive 47 Gene Set

From ClinVar Gene-Phenotype Associations

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

X-linked mental retardation 21 Gene Set

From ClinVar Gene-Phenotype Associations

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

Alacrima, achalasia, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, X-linked, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

X-linked mental retardation 30 Gene Set

From ClinVar Gene-Phenotype Associations

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

Mental retardation, X-linked, syndromic 10 Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

Siderius X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

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

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

From CTD Gene-Disease Associations

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

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.

Partington X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Alopecia-Mental Retardation Syndrome 1 Gene Set

From CTD Gene-Disease Associations

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

Alopecia-Mental Retardation Syndrome 2 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 30 Gene Set

From CTD Gene-Disease Associations

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

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 Retardation, Autosomal Recessive 13 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 23 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 91 Gene Set

From CTD Gene-Disease Associations

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

Miles-Carpenter x-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 95 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 9 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 77 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked, Syndromic 13 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked, Syndromic 12 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked, Syndromic 14 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

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

Lubs X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

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

Mental 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 Retardation, Fra12a Type Gene Set

From CTD Gene-Disease Associations

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

HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 20 Gene Set

From CTD Gene-Disease Associations

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

Mental retardation X-linked syndromic 7 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Dominant 3 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Dominant 5 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Dominant 4 Gene Set

From CTD Gene-Disease Associations

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

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.

Mental Retardation, X-Linked 17 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

X-linked mental retardation Gustavson type Gene Set

From CTD Gene-Disease Associations

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

Epilepsy, Female-Restricted, with Mental Retardation Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 81 Gene Set

From CTD Gene-Disease Associations

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

Mental retardation, X-linked 14 Gene Set

From CTD Gene-Disease Associations

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

Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 84 Gene Set

From CTD Gene-Disease Associations

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

Mental retardation, X-linked, syndromic 5 Gene Set

From CTD Gene-Disease Associations

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

BRACHYDACTYLY-MENTAL RETARDATION SYNDROME Gene Set

From CTD Gene-Disease Associations

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

Birk-Barel Mental Retardation Dysmorphism Syndrome Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

MENTAL RETARDATION, X-LINKED 21 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked, with Epilepsy Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 9 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 78 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 3 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 73 Gene Set

From CTD Gene-Disease Associations

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

Abidi X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 4 Gene Set

From CTD Gene-Disease Associations

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

Mental 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 Retardation, X-Linked 82 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 11 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 10 Gene Set

From CTD Gene-Disease Associations

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

MENTAL RETARDATION, X-LINKED 96 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 8 Gene Set

From CTD Gene-Disease Associations

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

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 2 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 7 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 6 Gene Set

From CTD Gene-Disease Associations

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

MENTAL RETARDATION, X-LINKED 49 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked, With Panhypopituitarism Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 52 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 53 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 58 Gene Set

From CTD Gene-Disease Associations

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

MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Recessive 1 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 63 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Armfield X-Linked Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 42 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 93 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 94 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Cleft Palate, Isolated, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Microcephaly with Mental Retardation and Digital Anomalies Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 72 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 45 Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 46 Gene Set

From CTD Gene-Disease Associations

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

Prieto X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked, Syndromic 10 Gene Set

From CTD Gene-Disease Associations

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

Martin-Probst Deafness-Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, X-Linked 50 Gene Set

From CTD Gene-Disease Associations

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

Cubitus Valgus with Mental Retardation and Unusual Facies Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Parkinsonism, early onset with mental retardation Gene Set

From CTD Gene-Disease Associations

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

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.

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.

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.

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.

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.

epilepsy; mental retardation Gene Set

From GAD Gene-Disease Associations

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

mental retardation; rett syndrome Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

language development disorders; mental retardation Gene Set

From GAD Gene-Disease Associations

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

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.

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.

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.

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

From GAD Gene-Disease Associations

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

mental retardation; muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

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

violent offenders with mental retardation Gene Set

From GAD Gene-Disease Associations

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

schizophrenia; mental retardation Gene Set

From GAD Gene-Disease Associations

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

leukomalacia, periventricular; mental retardation Gene Set

From GAD Gene-Disease Associations

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

mental 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 retardation; syndrome Gene Set

From GAD Gene-Disease Associations

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

non-syndromic x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

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

epilepsy and mental retardation Gene Set

From GAD Gene-Disease Associations

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

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.

brain diseases; mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

congenital abnormalities; mental retardation Gene Set

From GAD Gene-Disease Associations

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

learning disorders; memory disorders; mental retardation Gene Set

From GAD Gene-Disease Associations

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

x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

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

mental 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 retardation, x-linked Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

mental retardation, x-linked; syndrome Gene Set

From GAD Gene-Disease Associations

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

mental retardation; microcephaly Gene Set

From GAD Gene-Disease Associations

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

mental retardation Gene Set

From GAD Gene-Disease Associations

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

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.

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 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 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.

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.

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.

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.

Fragile X mental retardation protein family Gene Set

From InterPro Predicted Protein Domain Annotations

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

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

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive, 9/26 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 19 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 18 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 10 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 13 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 12 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 15 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 14 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 17 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 16 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 84 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 81 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 82 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 89 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 28 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 29 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 23 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 27 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 24 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal recessive 25 Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

mental retardation with language impairment and autistic features Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 30 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 9 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 1 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 5 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, autosomal dominant 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, snyder-robinson type Gene Set

From OMIM Gene-Disease Associations

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

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 30/47 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 30/47 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked syndromic 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked syndromic 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, siderius type Gene Set

From OMIM Gene-Disease Associations

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

alpha-thalassemia/mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-thalassemia/mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 40 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 40 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 44 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 44 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 46 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked, fraxe type Gene Set

From OMIM Gene-Disease Associations

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

mental retardation syndrome, x-linked, armfield type Gene Set

From OMIM Gene-Disease Associations

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

?mental retardation, x-linked, syndromic 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.

alacrima, achalasia, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alacrima, achalasia, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 2 Gene Set

From OMIM Gene-Disease Associations

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

hyperphosphatasia with mental retardation syndrome 3 Gene Set

From OMIM Gene-Disease Associations

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

hyperphosphatasia with mental retardation syndrome 1 Gene Set

From OMIM Gene-Disease Associations

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

hyperphosphatasia with mental retardation syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

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, syndromic, hedera type Gene Set

From OMIM Gene-Disease Associations

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

?mental retardation, x-linked 91 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 91 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 90 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 90 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 98 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 98 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

mental retardation-hypotonic facies syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

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

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal dominant 22 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal dominant 22 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 30 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 78 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 78 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 72 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 72 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 52 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 52 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 53 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 53 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 50 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 50 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 58 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 58 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, claes-jensen type Gene Set

From OMIM Gene-Disease Associations

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

waisman parkinsonism-mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 21/34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 21/34 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 31 Gene Set

From OMIM Gene-Disease Associations

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

?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

choroideremia, deafness, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the choroideremia, deafness, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 10/20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 10/20 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?stocco dos santos x-linked mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?stocco dos santos x-linked mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 19 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 14 Gene Set

From OMIM Gene-Disease Associations

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

birk-barel mental retardation dysmorphism syndrome Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 77 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 77 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 9 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 15 (cabezas type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 15 (cabezas type) phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

brachydactyly-mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked, with short stature Gene Set

From OMIM Gene-Disease Associations

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

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, autosomal recessive 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive 43 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 43 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, chudley-schwartz type, Gene Set

From OMIM Gene-Disease Associations

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

mental retardation, x-linked 92 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 92 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 93 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 93 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 96 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 96 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 97 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 97 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 94 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 94 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 95 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 95 phenotype from the curated OMIM Gene-Disease Associations dataset.

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

?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.

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 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 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.

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, 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.

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.

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.

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.

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.

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.

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.

Peroxisome biogenesis disorder 9B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 9B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 3A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia-like disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 8B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 8B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 8A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 8A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisomal fatty acyl-coa reductase 1 disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisomal fatty acyl-coa reductase 1 disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 7B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 7A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 7A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rett's disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rett's disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nijmegen breakage syndrome-like disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nijmegen breakage syndrome-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Platelet-type bleeding disorder 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Platelet-type bleeding disorder 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2k Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1P Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1v Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia-like disorder 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial platelet disorder with associated myeloid malignancy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type Ix Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 4B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 5A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 5A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 5B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1K Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1y Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1u Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1t Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 11A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 11A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 11B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 11B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bleeding disorder, platelet-type, 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bleeding disorder, platelet-type, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bleeding disorder, platelet-type, 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bleeding disorder, platelet-type, 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Otopalatodigital spectrum disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Otopalatodigital spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 13A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 13A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Speech-language disorder 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Speech-language disorder 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 6A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 6A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peroxisome biogenesis disorder 6B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peroxisome biogenesis disorder 6B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aortic valve disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aortic valve disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stereotypic Movement Disorder Gene Set

From CTD Gene-Disease Associations

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

Tobacco Use Disorder Gene Set

From CTD Gene-Disease Associations

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

Speech-Sound Disorder Gene Set

From CTD Gene-Disease Associations

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

Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.

Orthostatic Hypotensive Disorder, Streeten Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Orthostatic Hypotensive Disorder, Streeten Type from the curated CTD Gene-Disease Associations dataset.

Paroxysmal Extreme Pain Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal Extreme Pain Disorder from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.

Autistic Disorder Gene Set

From CTD Gene-Disease Associations

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

Transient Myeloproliferative Disorder of Down Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Transient Myeloproliferative Disorder of Down Syndrome from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIF Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation, type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.

NOG-Related-Symphalangism Spectrum Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOG-Related-Symphalangism Spectrum Disorder from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.

Conduct Disorder Gene Set

From CTD Gene-Disease Associations

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

Congenital disorder of glycosylation type 1G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.

Pigmentary Disorder, Reticulate, with Systemic Manifestations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pigmentary Disorder, Reticulate, with Systemic Manifestations from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder of Glycosylation, Type Io Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.

Bleeding Disorder, East Texas Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bleeding Disorder, East Texas Type from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type Im Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type In Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.

Bipolar Disorder Gene Set

From CTD Gene-Disease Associations

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

ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.

PEROXISOME BIOGENESIS DISORDER 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PEROXISOME BIOGENESIS DISORDER 2B from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 8 from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 9 from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.

Obsessive-Compulsive Disorder Gene Set

From CTD Gene-Disease Associations

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

Nijmegen Breakage Syndrome-Like Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nijmegen Breakage Syndrome-Like Disorder from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.

REM Sleep Behavior Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease REM Sleep Behavior Disorder from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.

Depressive Disorder, Major Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Depressive Disorder, Major from the curated CTD Gene-Disease Associations dataset.

Antisocial Personality Disorder Gene Set

From CTD Gene-Disease Associations

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

Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.

Myeloproliferative Disorder, Chronic, with Eosinophilia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myeloproliferative Disorder, Chronic, with Eosinophilia from the curated CTD Gene-Disease Associations dataset.

BLEEDING DISORDER, PLATELET-TYPE, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BLEEDING DISORDER, PLATELET-TYPE, 8 from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1F from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj from the curated CTD Gene-Disease Associations dataset.

Major Depressive Disorder 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Depressive Disorder 1 from the curated CTD Gene-Disease Associations dataset.

Major Depressive Disorder 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Depressive Disorder 2 from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 4 from the curated CTD Gene-Disease Associations dataset.

Attention Deficit Disorder with Hyperactivity Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Attention Deficit Disorder with Hyperactivity from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1K from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1L from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1C from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1E from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1D from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation, type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation, type 2G from the curated CTD Gene-Disease Associations dataset.

Depressive Disorder Gene Set

From CTD Gene-Disease Associations

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

Congenital Disorder Of Glycosylation, Type IIH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIH from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 2 from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 3 from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 1 from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 6 from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 7 from the curated CTD Gene-Disease Associations dataset.

Major Affective Disorder 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Major Affective Disorder 5 from the curated CTD Gene-Disease Associations dataset.

Panic Disorder Gene Set

From CTD Gene-Disease Associations

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

SPEECH-LANGUAGE DISORDER 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPEECH-LANGUAGE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIB from the curated CTD Gene-Disease Associations dataset.

Tobacco Use Disorder Gene Set

From dbGAP Gene-Trait Associations

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

Depressive Disorder, Major Gene Set

From dbGAP Gene-Trait Associations

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

Depressive Disorder Gene Set

From dbGAP Gene-Trait Associations

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

Autistic Disorder Gene Set

From dbGAP Gene-Trait Associations

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

Conduct Disorder Gene Set

From dbGAP Gene-Trait Associations

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

Panic Disorder Gene Set

From dbGAP Gene-Trait Associations

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

Bipolar Disorder Gene Set

From dbGAP Gene-Trait Associations

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

Attention Deficit Disorder with Hyperactivity Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Attention Deficit Disorder with Hyperactivity in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

congenital disorder of glycosylation Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease congenital disorder of glycosylation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

carbohydrate metabolic disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cognitive disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

metal metabolism disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

glycogen metabolism disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

urea cycle disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

physical disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

gamma-amino butyric acid metabolism disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease gamma-amino butyric acid metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

tic disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

purine-pyrimidine metabolic disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease purine-pyrimidine metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

sleep disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

bilirubin metabolic disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

amino acid metabolic disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease amino acid metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

inherited metabolic disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

lipid metabolism disorder Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

psychotic disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

sexual disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

cognitive disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

mood disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

conduct disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

substance-related disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

physical disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

impulse control disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

attention deficit hyperactivity disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease attention deficit hyperactivity disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

inherited metabolic disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

bipolar disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

panic disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

eating disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

tic disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

sleep disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

autistic disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

autism spectrum disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

lipid metabolism disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

personality disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

anxiety disorder Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

stereotypic movement disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bipolar disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital disorder of glycosylation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

body dysmorphic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital disorder of glycosylation type ii Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease congenital disorder of glycosylation type ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

somatization disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cyclothymic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

paraphilia disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

lipid metabolism disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

panic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

histrionic personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

psychotic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

schizotypal personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sexual disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

carbohydrate metabolic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vitamin metabolic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

mood disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

neurotic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

conduct disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

post-traumatic stress disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

chronic tic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

urea cycle disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

avoidant personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

glycogen metabolism disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dysthymic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

periodic limb movement disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

combat disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

expressive language disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gender identity disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autism spectrum disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

purine-pyrimidine metabolic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

amino acid metabolic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

paranoid personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

schizoaffective disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sleep disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

borderline personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

obsessive-compulsive disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

articulation disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anxiety disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

psychosexual disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

antisocial personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dependent personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

somatoform disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

steroid inherited metabolic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

generalized anxiety disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

metal metabolism disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dissociative disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

schizoid personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fetal alcohol spectrum disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

substance-related disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

physical disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

communication disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

intermittent explosive disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

speech disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autistic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

attention deficit hyperactivity disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bipolar i disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

inherited metabolic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

obsessive-compulsive personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

schizophreniform disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alcohol-related neurodevelopmental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

amnestic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

reading disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

writing disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bilirubin metabolic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

language disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cognitive disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

seasonal affective disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

eating disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

rumination disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

withdrawal disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

impulse control disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

delusional disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

major depressive disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute stress disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypoactive sexual desire disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pain disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

phobic disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

narcissistic personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital disorder of glycosylation type i Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease congenital disorder of glycosylation type i in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

adjustment disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gamma-amino butyric acid metabolism disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease gamma-amino butyric acid metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

factitious disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

atypical depressive disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

separation anxiety disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

obsessive compulsive disorder Gene Set

From GAD Gene-Disease Associations

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

depressive disorder, major; alcoholism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depressive disorder, major; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; depressive disorder, major Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; depressive disorder, major in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit hyperactivity disorder Gene Set

From GAD Gene-Disease Associations

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

schizophrenia; alcoholism; bipolar disorder Gene Set

From GAD Gene-Disease Associations

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

schizophrenia; bipolar disorder; psychoses Gene Set

From GAD Gene-Disease Associations

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

body weight; seasonal affective disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung neoplasms; neoplasm of lung ; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

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

carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

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

conduct disorder (interaction) Gene Set

From GAD Gene-Disease Associations

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

obsessive-compulsive disorder Gene Set

From GAD Gene-Disease Associations

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

anxiety disorder Gene Set

From GAD Gene-Disease Associations

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

anxiety disorder; blood pressure, arterial; memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety disorder; blood pressure, arterial; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

visual disorder Gene Set

From GAD Gene-Disease Associations

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

posttraumatic stress disorder Gene Set

From GAD Gene-Disease Associations

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

alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypercholesterolemia; h. pylori infection; coagulation disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypercholesterolemia; h. pylori infection; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adhd ; attention-deficit hyperactivity disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adhd ; attention-deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

major depressive disorder (broad) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease major depressive disorder (broad) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

post-traumatic stress disorder Gene Set

From GAD Gene-Disease Associations

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

bipolar and unipolar disorder Gene Set

From GAD Gene-Disease Associations

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

bipolar schizoaffective disorder Gene Set

From GAD Gene-Disease Associations

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

amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amino acid disorder, nos; amino acid metabolism, inborn errors; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy complications; tic disorder; tic disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy complications; tic disorder; tic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head and neck neoplasms; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antisocial behavior conduct disorder Gene Set

From GAD Gene-Disease Associations

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

obesity; affective disorder Gene Set

From GAD Gene-Disease Associations

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

disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; bipolar disorder Gene Set

From GAD Gene-Disease Associations

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

pregnancy loss, recurrent; coagulation disorder Gene Set

From GAD Gene-Disease Associations

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

bipolar disorder; mania, antidepressant-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bipolar disorder; mania, antidepressant-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

porphyrias; porphyrin disorder Gene Set

From GAD Gene-Disease Associations

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

mood disorder Gene Set

From GAD Gene-Disease Associations

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

opioid-related disorders; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease opioid-related disorders; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; autism; alcoholism; attention deficit hyperactivity disorder; cocaine abuse; psychosis, puerperal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; autism; alcoholism; attention deficit hyperactivity disorder; cocaine abuse; psychosis, puerperal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety disorder; alcoholism; depression; narcolepsy Gene Set

From GAD Gene-Disease Associations

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

obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

seasonal affective disorder Gene Set

From GAD Gene-Disease Associations

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

attention-deficit/hyperactivity disorder Gene Set

From GAD Gene-Disease Associations

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

major depressive disorder Gene Set

From GAD Gene-Disease Associations

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

obsessive- compulsive disorder Gene Set

From GAD Gene-Disease Associations

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

alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-related disorders; carcinoma, squamous cell; head and neck neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia ; depression ; bipolar disorder Gene Set

From GAD Gene-Disease Associations

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

bipolar affective disorder Gene Set

From GAD Gene-Disease Associations

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

carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; mouth neoplasms; squamous cell carcinoma; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety disorder; alcoholism Gene Set

From GAD Gene-Disease Associations

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

eating disorder Gene Set

From GAD Gene-Disease Associations

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

disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit hyperactivity disorder-like phenotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit hyperactivity disorder-like phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bipolar affective disorder. Gene Set

From GAD Gene-Disease Associations

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

attention deficit hyperactivity disorder; reading disability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit hyperactivity disorder; reading disability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety disorder; depression Gene Set

From GAD Gene-Disease Associations

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

impulse control disorder Gene Set

From GAD Gene-Disease Associations

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

natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autistic disorder Gene Set

From GAD Gene-Disease Associations

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

schizophrenia; panic disorder Gene Set

From GAD Gene-Disease Associations

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

mood disorder. Gene Set

From GAD Gene-Disease Associations

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

anxiety disorder; alcohol abuse Gene Set

From GAD Gene-Disease Associations

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

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depressive disorder, major; nausea Gene Set