Name

Epileptic encephalopathy, childhood-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

epileptic encephalopathy, childhood-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infanitle, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the epileptic encephalopathy, early infanitle, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Early infantile epileptic encephalopathy 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early infantile epileptic encephalopathy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 25 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 26 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic encephalopathy, early infantile, 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epileptic encephalopathy, early infantile, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epileptic Encephalopathy, Early Infantile, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 4 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 1 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 2 from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7 from the curated CTD Gene-Disease Associations dataset.

Epileptic encephalopathy, Lennox-Gastaut type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic encephalopathy, Lennox-Gastaut type from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11 from the curated CTD Gene-Disease Associations dataset.

Epileptic Encephalopathy, Early Infantile, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epileptic Encephalopathy, Early Infantile, 3 from the curated CTD Gene-Disease Associations dataset.

EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12 from the curated CTD Gene-Disease Associations dataset.

epileptic encephalopathy Gene Set

From HPO Gene-Disease Associations

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

epileptic encephalopathy, early infantile, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

epileptic encephalopathy, early infantile, 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epileptic encephalopathy, early infantile, 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

?epileptic encephalopathy, early infantile, 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epileptic encephalopathy, early infantile, 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

Myopathy, reducing body, X-linked, childhood-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset.

childhood-onset mood disorders Gene Set

From GAD Gene-Disease Associations

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

asthma (childhood onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma (childhood onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Asthma (childhood onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

childhood-onset short-trunk short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

childhood onset Gene Set

From HPO Gene-Disease Associations

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

childhood-onset truncal obesity Gene Set

From HPO Gene-Disease Associations

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

childhood onset short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

childhood onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

myopathy, reducing body, x-linked, childhood-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

polyarteritis nodosa, childhood-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyarteritis nodosa, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

?neurodegeneration with optic atrophy, childhood onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.

adult-onset still disease; still's disease, adult-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult-onset still disease; still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epileptic Gene Set

From GeneRIF Biological Term Annotations

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

epileptic spasms Gene Set

From HPO Gene-Disease Associations

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

North american indian childhood cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the North american indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alternating hemiplegia of childhood Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercalciuria, childhood, self-limiting Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercalciuria, childhood, self-limiting phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Childhood hypophosphatasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alternating hemiplegia of childhood 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alternating hemiplegia of childhood 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

North American Indian Childhood Cirrhosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease North American Indian Childhood Cirrhosis from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophies of Childhood Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood 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.

Alternating hemiplegia of childhood Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alternating hemiplegia of childhood from the curated CTD Gene-Disease Associations dataset.

Arthropathy, progressive pseudorheumatoid, of childhood Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arthropathy, progressive pseudorheumatoid, of childhood from the curated CTD Gene-Disease Associations dataset.

Hypophosphatasia, Childhood Gene Set

From CTD Gene-Disease Associations

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

alternating hemiplegia of childhood Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

childhood medulloblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood oligodendroglioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood electroclinical syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood type dermatomyositis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood kidney neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood disintegrative disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood malignant schwannoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood kidney cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood endodermal sinus tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood absence epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alternating hemiplegia of childhood Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

childhood pilocytic astrocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

severe childhood thrombosis Gene Set

From GAD Gene-Disease Associations

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

childhood leukemia Gene Set

From GAD Gene-Disease Associations

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

childhood b-cell non-hodgkin's lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease childhood b-cell non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphoblastic leukemia (childhood) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphoblastic leukemia (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood asthma Gene Set

From GAD Gene-Disease Associations

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

childhood obesity Gene Set

From GAD Gene-Disease Associations

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

bronchial asthma (childhood only) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchial asthma (childhood only) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

temperament in early childhood Gene Set

From GAD Gene-Disease Associations

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

arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood absence epilepsy. Gene Set

From GAD Gene-Disease Associations

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

childhood b-cell precursor acute lymphoblastic leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease childhood b-cell precursor acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophies of childhood Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood brain tumors ; residential insecticide exposure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease childhood brain tumors ; residential insecticide exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchial asthma (childhood & adult) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchial asthma (childhood & adult) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood atopic asthma Gene Set

From GAD Gene-Disease Associations

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

arthritis, juvenile rheumatoid; chronic childhood arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood brain tumor Gene Set

From GAD Gene-Disease Associations

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

leukemia, childhood acute lymphoblastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, childhood acute lymphoblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood acute lymphoblastic leukemia Gene Set

From GAD Gene-Disease Associations

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

childhood maltreatment Gene Set

From GAD Gene-Disease Associations

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

childhood asthma. Gene Set

From GAD Gene-Disease Associations

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

asthma (childhood) Gene Set

From GAD Gene-Disease Associations

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

leukemia, childhood acute; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, childhood acute; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood idiopathic thrombocytopenic purpura. Gene Set

From GAD Gene-Disease Associations

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

asthma and ige in childhood Gene Set

From GAD Gene-Disease Associations

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

arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

childhood Gene Set

From GeneRIF Biological Term Annotations

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

Fractional exhaled nitric oxide (childhood) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Acute lymphoblastic leukemia (childhood) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Intelligence (childhood) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Intelligence (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Asthma (childhood, severe) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Asthma (childhood, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

recurrent infections in infancy and early childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

death in childhood Gene Set

From HPO Gene-Disease Associations

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

loss of ability to walk in early childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inability to walk by childhood/adolescence Gene Set

From HPO Gene-Disease Associations

genes associated with the inability to walk by childhood/adolescence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

platyspondyly (childhood) Gene Set

From HPO Gene-Disease Associations

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

Spinal Muscular Atrophies of Childhood Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Lead Poisoning, Nervous System, Childhood Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Lead Poisoning, Nervous System, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Schizophrenia, Childhood Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

hypophosphatasia, childhood Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypophosphatasia, childhood phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatocellular carcinoma, childhood type Gene Set

From OMIM Gene-Disease Associations

genes associated with the hepatocellular carcinoma, childhood type phenotype from the curated OMIM Gene-Disease Associations dataset.

alternating hemiplegia of childhood 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alternating hemiplegia of childhood 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, childhood absence, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

transient erythroblastopenia of childhood Gene Set

From OMIM Gene-Disease Associations

genes associated with the transient erythroblastopenia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, childhood absence, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, childhood absence, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, childhood absence, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, childhood absence, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

cirrhosis, north american indian childhood type Gene Set

From OMIM Gene-Disease Associations

genes associated with the cirrhosis, north american indian childhood type phenotype from the curated OMIM Gene-Disease Associations dataset.

alternating hemiplegia of childhood Gene Set

From OMIM Gene-Disease Associations

genes associated with the alternating hemiplegia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.

arthropathy, progressive pseudorheumatoid, of childhood Gene Set

From OMIM Gene-Disease Associations

genes associated with the arthropathy, progressive pseudorheumatoid, of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.

{epilepsy, childhood absence, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

Early myoclonic encephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Early myoclonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial encephalopathy with neuroserpin inclusion bodies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ethylmalonic encephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ethylmalonic encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertensive Encephalopathy Gene Set

From CTD Gene-Disease Associations

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

Hepatic Encephalopathy Gene Set

From CTD Gene-Disease Associations

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

ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

Wernicke Encephalopathy Gene Set

From CTD Gene-Disease Associations

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

Familial encephalopathy with neuroserpin inclusion bodies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.

Mitochondrial neurogastrointestinal encephalopathy syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mitochondrial neurogastrointestinal encephalopathy syndrome from the curated CTD Gene-Disease Associations dataset.

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset.

Spongiform Encephalopathy with Neuropsychiatric Features Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spongiform Encephalopathy with Neuropsychiatric Features from the curated CTD Gene-Disease Associations dataset.

Ethylmalonic encephalopathy Gene Set

From CTD Gene-Disease Associations

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

glycine encephalopathy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

glycine encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hepatic encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

early myoclonic encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

wernicke encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

toxic encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypertensive encephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

chronic toxic encephalopathy Gene Set

From GAD Gene-Disease Associations

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

hepatic encephalopathy; liver cirrhosis Gene Set

From GAD Gene-Disease Associations

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

encephalopathy Gene Set

From GeneRIF Biological Term Annotations

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

MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MELAS - Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes_Muscle - Striated (Skeletal) (MMHCC)_GSE1462 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

hypoglycemic encephalopathy Gene Set

From HPO Gene-Disease Associations

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

progressive encephalopathy Gene Set

From HPO Gene-Disease Associations

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

recurrent encephalopathy Gene Set

From HPO Gene-Disease Associations

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

hepatic encephalopathy Gene Set

From HPO Gene-Disease Associations

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

encephalopathy Gene Set

From HPO Gene-Disease Associations

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

acute encephalopathy Gene Set

From HPO Gene-Disease Associations

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

infantile encephalopathy Gene Set

From HPO Gene-Disease Associations

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

mitochondrial encephalopathy Gene Set

From HPO Gene-Disease Associations

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

acute necrotizing encephalopathy Gene Set

From HPO Gene-Disease Associations

genes associated with the acute necrotizing encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hepatic Encephalopathy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Encephalopathy, Bovine Spongiform Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

spongiform encephalopathy Gene Set

From MPO Gene-Phenotype Associations

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

{encephalopathy, acute, infection-induced, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 3, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 3, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 4, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 4, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

ethylmalonic encephalopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ethylmalonic encephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopathy, familial, with neuroserpin inclusion bodies Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopathy, familial, with neuroserpin inclusion bodies phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopathy, neonatal severe Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopathy, neonatal severe phenotype from the curated OMIM Gene-Disease Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

glycine encephalopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the glycine encephalopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopathy, progressive, with or without lipodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective ACY1 causes encephalopathy Gene Set

From Reactome Pathways

proteins participating in the Defective ACY1 causes encephalopathy pathway from the Reactome Pathways dataset.

CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SCID due to ADA deficiency, delayed onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, reducing body, X-linked, early-onset, severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma, primary open angle, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma, primary open angle, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gm2-gangliosidosis, adult-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gm2-gangliosidosis, adult-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 20, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 20, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sarcoidosis, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sarcoidosis, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 6, autosomal recessive early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 6, autosomal recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular degeneration, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular degeneration, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Breast cancer, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Breast cancer, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 19, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 19, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile-onset dystonia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult onset ataxia with oculomotor apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult onset ataxia with oculomotor apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile-onset ascending hereditary spastic paralysis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, early-onset severe Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-onset diabetes of the young, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Maturity-onset diabetes of the young, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sting-associated vasculopathy, infantile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sting-associated vasculopathy, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune disease, multisystem, infantile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune disease, multisystem, infantile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary open angle glaucoma juvenile onset 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary open angle glaucoma juvenile onset 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Maturity-Onset Diabetes of the Young, Type 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 7 from the curated CTD Gene-Disease Associations dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.

Neonatal-onset citrullinemia type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neonatal-onset citrullinemia type 2 from the curated CTD Gene-Disease Associations dataset.

Myopathy, Distal, with Anterior Tibial Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 1 from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 2 from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 4 from the curated CTD Gene-Disease Associations dataset.

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Carnitine Palmitoyltransferase II Deficiency, Late-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carnitine Palmitoyltransferase II Deficiency, Late-Onset from the curated CTD Gene-Disease Associations dataset.

Hereditary spastic paralysis, infantile onset ascending Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.

MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10 from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes Of The Young, Type 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes Of The Young, Type 9 from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE, LATE-ONSET Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE, LATE-ONSET from the curated CTD Gene-Disease Associations dataset.

Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset.

Maturity-Onset Diabetes of the Young, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 3 from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 6, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

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

Cataract, Autosomal Recessive, Early-Onset, Pulverulent Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Recessive, Early-Onset, Pulverulent from the curated CTD Gene-Disease Associations dataset.

Sarcoidosis, Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sarcoidosis, Early-Onset from the curated CTD Gene-Disease Associations dataset.

Juvenile-onset dystonia Gene Set

From CTD Gene-Disease Associations

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

Albinism ocular late onset sensorineural deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Albinism ocular late onset sensorineural deafness from the curated CTD Gene-Disease Associations dataset.

Cataract, Cortical, Juvenile-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Cortical, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.

Adult-onset citrullinemia type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adult-onset citrullinemia type 2 from the curated CTD Gene-Disease Associations dataset.

Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type from the curated CTD Gene-Disease Associations dataset.

Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset.

MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11 from the curated CTD Gene-Disease Associations dataset.

Cataract, Pulverulent, Juvenile-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Pulverulent, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.

Myopathy, Early-Onset, with Fatal Cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Early-Onset, with Fatal Cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

Late-Onset Retinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Late-Onset Retinal Degeneration 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.

Parkinson Disease 7, Autosomal Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

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

Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset.

infantile onset spinocerebellar ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease infantile onset spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

variable age at onset electroclinical syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease variable age at onset electroclinical syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

infantile onset spinocerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

maturity-onset diabetes of the young Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

adult-onset still's disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease adult-onset still's disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

variable age at onset electroclinical syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease variable age at onset electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

early onset absence epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

adult onset multi/minicore myopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult onset multi/minicore myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

still's disease, adult-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease still's disease, adult-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sporadic adult-onset lower motor neuron disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sporadic adult-onset lower motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

respiratory papillomatosis, juvenile-onset; recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease respiratory papillomatosis, juvenile-onset; recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

maturity onset diabetes of the young Gene Set

From GAD Gene-Disease Associations

genes associated with the disease maturity onset diabetes of the young in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menarche and menopause (age at onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarche and menopause (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delayed onset of glycogenosis type ii. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease delayed onset of glycogenosis type ii. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset alcoholism/substance abuse. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset alcoholism/substance abuse. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrence and early onset of venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrence and early onset of venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis (age of onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory bowel disease (early onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory bowel disease (early onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset familial alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-onset familial alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

periodontitis, early-onset Gene Set

From GAD Gene-Disease Associations

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

late-onset airflow obstruction Gene Set

From GAD Gene-Disease Associations

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

menarche (age at onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarche (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset prostate cancer Gene Set

From GAD Gene-Disease Associations

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

puberty onset Gene Set

From GAD Gene-Disease Associations

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

late-onset vascular disease Gene Set

From GAD Gene-Disease Associations

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

citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease citrullinemia, adult-onset type ii; hepatitis, neonatal associated with cholestasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset airflow Gene Set

From GAD Gene-Disease Associations

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

late-onset stargardt disease Gene Set

From GAD Gene-Disease Associations

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

late onset of familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late onset of familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset alcoholism Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

myocardial infarction (early onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction (early onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, early-onset Gene Set

From GAD Gene-Disease Associations

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

familial early onset psoriasis. Gene Set

From GAD Gene-Disease Associations

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

obesity (early onset extreme) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity (early onset extreme) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset of sudden infant death. Gene Set

From GAD Gene-Disease Associations

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

citrullinemia, adult-onset type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease citrullinemia, adult-onset type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset ischemic heart disease. Gene Set

From GAD Gene-Disease Associations

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

parkinson's disease (age of onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adolescent-onset antisocial behavior Gene Set

From GAD Gene-Disease Associations

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

late-onset alport syndrome Gene Set

From GAD Gene-Disease Associations

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

late onset familial adenomatous polyposis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late onset familial adenomatous polyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late-onset congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset aggressive diffuse amyloidosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early-onset aggressive diffuse amyloidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset glycogen storage disease type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late-onset glycogen storage disease type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bulbar-onset motor neuron disease Gene Set

From GAD Gene-Disease Associations

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

late-onset ad Gene Set

From GAD Gene-Disease Associations

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

dystonia, early onset primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease (late onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease (late onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menopause (age at onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menopause (age at onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset alzheimer's disease. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late-onset alzheimer's disease. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset periodontitis Gene Set

From GAD Gene-Disease Associations

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

hypertension (young onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension (young onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infantile-onset ascending hereditary spastic paralysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

variable age at onset disease Gene Set

From GAD Gene-Disease Associations

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

early onset of multiple sclerosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of multiple sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit hyperactivity disorder (time to onset) Gene Set

From GAD Gene-Disease Associations

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

late-onset alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late-onset alzheimer's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial hypertension of early onset. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial hypertension of early onset. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early-onset periodontitis Gene Set

From GAD Gene-Disease Associations

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

onsetrelated Gene Set

From GeneRIF Biological Term Annotations

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

onset Gene Set

From GeneRIF Biological Term Annotations

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

onsets Gene Set

From GeneRIF Biological Term Annotations

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

Amyotrophic lateral sclerosis (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Alzheimer's disease (late onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Alzheimer's disease (late onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Prostate cancer (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Prostate cancer (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Menarche and menopause (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Menarche and menopause (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Puberty onset (genital enlargement) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Puberty onset (genital enlargement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Alcohol dependence (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Alcohol dependence (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Obesity (early onset extreme) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Obesity (early onset extreme) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Menopause (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Menopause (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Menarche (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Femoral neck bone geometry and menarche (age at onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Inflammatory bowel disease (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Inflammatory bowel disease (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bipolar disorder (age of onset and psychomotor symptoms) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bipolar disorder (age of onset and psychomotor symptoms) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Puberty onset Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Alzheimer's disease (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Alzheimer's disease (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Puberty onset (breast development) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Puberty onset (breast development) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Narcolepsy (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Narcolepsy (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Myocardial infarction (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Myocardial infarction (early onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Breast cancer (early onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Attention deficit hyperactivity disorder (time to onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Attention deficit hyperactivity disorder (time to onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Parkinson's disease (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Parkinson's disease (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

late-onset distal muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the late-onset distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

middle age onset Gene Set

From HPO Gene-Disease Associations

genes associated with the middle age onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

young adult onset Gene Set

From HPO Gene-Disease Associations

genes associated with the young adult onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

late-onset proximal muscle weakness Gene Set

From HPO Gene-Disease Associations

genes associated with the late-onset proximal muscle weakness 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.

infantile onset Gene Set

From HPO Gene-Disease Associations

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

insidious onset Gene Set

From HPO Gene-Disease Associations

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

late-onset spinocerebellar degeneration Gene Set

From HPO Gene-Disease Associations

genes associated with the late-onset spinocerebellar degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

joint swelling onset late infancy Gene Set

From HPO Gene-Disease Associations

genes associated with the joint swelling onset late infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

maturity-onset diabetes of the young Gene Set

From HPO Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

late onset Gene Set

From HPO Gene-Disease Associations

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

adult onset Gene Set

From HPO Gene-Disease Associations

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

onset Gene Set

From HPO Gene-Disease Associations

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

adult-onset night blindness Gene Set

From HPO Gene-Disease Associations

genes associated with the adult-onset night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

late onset congenital glaucoma Gene Set

From HPO Gene-Disease Associations

genes associated with the late onset congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

early onset of sexual maturation Gene Set

From HPO Gene-Disease Associations

genes associated with the early onset of sexual maturation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adult onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the adult onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile onset Gene Set

From HPO Gene-Disease Associations

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

neonatal onset Gene Set

From HPO Gene-Disease Associations

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

congenital onset Gene Set

From HPO Gene-Disease Associations

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

Still's Disease, Adult-Onset Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Still's Disease, Adult-Onset phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

maturity onset diabetes of the young Gene Set

From KEGG Pathways

proteins participating in the maturity onset diabetes of the young pathway from the KEGG Pathways dataset.

late onset of menarche Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the late onset of menarche phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

macular degeneration, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular degeneration, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1b, primary open angle, adult onset, Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1b, primary open angle, adult onset, phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset severe Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset severe phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal degeneration, late-onset, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, early-onset, with fatal cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, early-onset, with fatal cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

{osteoporosis, early-onset, susceptibility to, autosomal dominant} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {osteoporosis, early-onset, susceptibility to, autosomal dominant} phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract with late-onset corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type viii Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type viii phenotype from the curated OMIM Gene-Disease Associations dataset.

obesity, mild, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity, mild, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 19, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 19, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

breast cancer, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the breast cancer, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{parkinson disease, late-onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {parkinson disease, late-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type ix Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type ix phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease 9, late onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease 9, late onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

hepatic failure, early onset, and neurologic disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the hepatic failure, early onset, and neurologic disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

cystinosis, late-onset juvenile or adolescent nephropathic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cystinosis, late-onset juvenile or adolescent nephropathic phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ceroid lipofuscinosis, neuronal, kufs type, adult onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the ceroid lipofuscinosis, neuronal, kufs type, adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.

inflammatory bowel disease 25, early onset, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inflammatory bowel disease 25, early onset, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

{bulimia nervosa, age of onset of weight loss in} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bulimia nervosa, age of onset of weight loss in} phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type vii Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type vii phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, early-onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, early-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, late-onset, finkel type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

sting-associated vasculopathy, infantile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the sting-associated vasculopathy, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, adult-onset, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, adult-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

fanconi renotubular syndrome 4, with maturity-onset diabetes of the young Gene Set

From OMIM Gene-Disease Associations

genes associated with the fanconi renotubular syndrome 4, with maturity-onset diabetes of the young phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young, type 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young, type 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

citrullinemia, adult-onset type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the citrullinemia, adult-onset type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

chondrocalcinosis with early-onset osteoarthritis Gene Set

From OMIM Gene-Disease Associations

genes associated with the chondrocalcinosis with early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.

inflammatory bowel disease 28, early onset, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inflammatory bowel disease 28, early onset, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

{obesity, late-onset} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {obesity, late-onset} phenotype from the curated OMIM Gene-Disease Associations dataset.

sarcoidosis, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the sarcoidosis, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease, late-onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease, late-onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease, late-onset} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease, late-onset} phenotype from the curated OMIM Gene-Disease Associations dataset.

{major affective disorder 3, early onset} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {major affective disorder 3, early onset} phenotype from the curated OMIM Gene-Disease Associations dataset.

maturity-onset diabetes of the young 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the maturity-onset diabetes of the young 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteochondritis dissecans, short stature, and early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.

diabetes mellitus, noninsulin-dependent, late onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the diabetes mellitus, noninsulin-dependent, late onset phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 6, early onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 6, early onset phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset, and pituitary dysfunction Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperchylomicronemia, late-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperchylomicronemia, late-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

citrullinemia, type ii, neonatal-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the citrullinemia, type ii, neonatal-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1k, primary open angle, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1k, primary open angle, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, distal, with anterior tibial onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 3a, primary open angle, congenital, juvenile, or adult onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 3a, primary open angle, congenital, juvenile, or adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 7, autosomal recessive early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 7, autosomal recessive early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 20, early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 20, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary disease, chronic obstructive, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary disease, chronic obstructive, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease 19, late onset, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease 19, late onset, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, reducing body, x-linked, severe early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, reducing body, x-linked, severe early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune disease, multisystem, infantile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune disease, multisystem, infantile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, early-onset atypical, with myoclonic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paralysis, infantile onset ascending Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.

Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components Gene Set

From Reactome Pathways

proteins participating in the Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components pathway from the Reactome Pathways dataset.