Name

alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; lewy body disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dementia; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; dementia, vascular; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; dementia, vascular Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; parkinson disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; dementia, vascular; lewy body disease; pick disease of the brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

Supranuclear Palsy, Progressive, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Supranuclear Palsy, Progressive, 2 from the curated CTD Gene-Disease Associations dataset.

Supranuclear Palsy, Progressive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Supranuclear Palsy, Progressive, 3 from the curated CTD Gene-Disease Associations dataset.

Supranuclear Palsy, Progressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Supranuclear Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.

Progressive supranuclear palsy atypical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive supranuclear palsy atypical from the curated CTD Gene-Disease Associations dataset.

Supranuclear Palsy, Progressive Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Supranuclear Palsy, Progressive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

progressive supranuclear palsy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

progressive supranuclear palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial atypical progressive supranuclear palsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

progressive supranuclear palsy Gene Set

From GAD Gene-Disease Associations

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

neurodegenerative diseases; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

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

brain diseases; neurodegenerative diseases; supranuclear palsy, progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain diseases; neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Progressive supranuclear palsy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

progressive supranuclear palsy Gene Set

From GWASdb SNP-Disease Associations

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

Supranuclear Palsy, Progressive Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

supranuclear palsy, progressive, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

supranuclear palsy, progressive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

supranuclear palsy, progressive atypical Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive atypical phenotype from the curated OMIM Gene-Disease Associations dataset.

supranuclear palsy, progressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the supranuclear palsy, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease; dementia; neurodegenerative diseases; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; neurodegenerative diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; diabetes mellitus; hypercholesterolemia; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia, vascular Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebrovascular disorders; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; central nervous system diseases; parkinson disease; parkinsonian disorders; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; dementia, vascular; lipid metabolism disorders; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; dementia, vascular; lipid metabolism disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; mercury poisoning, nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; mercury poisoning, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; disease progression Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; cardiovascular diseases; chronic disease Gene Set

From GAD Gene-Disease Associations

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

supranuclear gaze palsy Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the supranuclear gaze palsy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

vertical supranuclear gaze palsy Gene Set

From HPO Gene-Disease Associations

genes associated with the vertical supranuclear gaze palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

supranuclear gaze palsy Gene Set

From HPO Gene-Disease Associations

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

horizontal supranuclear gaze palsy Gene Set

From HPO Gene-Disease Associations

genes associated with the horizontal supranuclear gaze palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease 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.

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.

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.

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.

?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.

?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.

parkinson's disease ; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; parkinson's disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease parkinson's disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; insulin; lung function; depression; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; coronary artery disease; diabetes, type 2; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol amnestic disorder; alcoholism; alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; olfaction disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; encephalitis, herpes simplex; herpes encephalitis Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; memory disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; myocardial ischemia Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cerebral amyloid angiopathy; cerebral infarction; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amnesia Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; metabolic diseases Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug toxicity; edema; nasopharyngitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; down syndrome; olfaction disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; hemochromatosis Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; arteriosclerosis Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; amyloidosis Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; brain infarction; cerebrovascular disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; delirium; recurrence Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; hallucinations Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; cardiovascular diseases; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; sclerosis Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal dementia, ubiquitin-positive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontotemporal dementia, ubiquitin-positive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

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

Frontotemporal Dementia, Chromosome 3-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Frontotemporal Dementia, Chromosome 3-Linked from the curated CTD Gene-Disease Associations dataset.

frontotemporal dementia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

frontotemporal dementia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia, frontotemporal Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; frontotemporal dementia; parkinsonian disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; frontotemporal dementia; parkinsonian disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia Gene Set

From GAD Gene-Disease Associations

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

frontotemporal dementia Gene Set

From GWASdb SNP-Disease Associations

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

frontotemporal dementia Gene Set

From HPO Gene-Disease Associations

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

Frontotemporal Dementia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, frontotemporal, with or without parkinsonism Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, frontotemporal, with or without parkinsonism phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, frontotemporal Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, frontotemporal phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis and/or frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis and/or frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis; dementia; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; dementia; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease; dementia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atropy Gene Set

From GeneRIF Biological Term Annotations

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

gaucher disease; nervous system diseases; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gaucher disease; nervous system diseases; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; aids dementia complex; aids related dementia complex; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; dementia; Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; dementia; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; vascular dementia Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; dementia Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; dementia Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; dementia; Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease and vascular dementia Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; dementia, vascular Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; hypothyroidism; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; hypothyroidism; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Gaze palsy, familial horizontal, with progressive scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.

Bulbar Palsy, Progressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bulbar Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.

progressive bulbar palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Bulbar Palsy, Progressive Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

gaze palsy, horizontal, with progressive scoliosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the gaze palsy, horizontal, with progressive scoliosis phenotype from the curated OMIM Gene-Disease Associations dataset.

aids dementia complex; aids related dementia complex Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids dementia complex; aids related dementia complex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; multiple sclerosis; hiv Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; multiple sclerosis; hiv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple cranial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

aphasia, primary progressive; dementia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aphasia, primary progressive; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, chronic progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, chronic progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Multiple Sclerosis, Chronic Progressive Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Sclerosis, Chronic Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

lewy body disease; parkinson disease Gene Set

From GAD Gene-Disease Associations

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

central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease central nervous system neoplasms; central nervous system tumors; hiv infections; lymphoma, aids-related; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aphasia, primary progressive; heredodegenerative disorders, nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aphasia, primary progressive; heredodegenerative disorders, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; multiple trauma; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; multiple trauma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; vascular disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; coronary artery disease; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; arthritis; lupus erythematosus; inflammatory bowel disease; insulin; malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease/coronary artery disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; lewy body disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; lewy body disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; atrophy; disease progression Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; chronic obstructive pulmonary disease/copd Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; chronic obstructive pulmonary disease/copd in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; disease progression Gene Set

From GAD Gene-Disease Associations

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

supranuclear Gene Set

From GeneRIF Biological Term Annotations

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

supranuclear ophthalmoplegia Gene Set

From HPO Gene-Disease Associations

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

multiple system atrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

multiple system atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

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

From GAD Gene-Disease Associations

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

multiple system atrophy Gene Set

From GAD Gene-Disease Associations

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

dystonic disorders; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple system atophy Gene Set

From GAD Gene-Disease Associations

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

Multiple System Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

{multiple system atrophy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED from the curated CTD Gene-Disease Associations dataset.

Frontotemporal Lobar Degeneration Gene Set

From CTD Gene-Disease Associations

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

frontotemporal lobar degeneration Gene Set

From GAD Gene-Disease Associations

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

frontotemporal Gene Set

From GeneRIF Biological Term Annotations

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

frontotemporal cerebral atrophy Gene Set

From HPO Gene-Disease Associations

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

Frontotemporal Lobar Degeneration Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

frontotemporal lobar degeneration, tardbp-related Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontotemporal lobar degeneration, tardbp-related phenotype from the curated OMIM Gene-Disease Associations dataset.

frontotemporal lobar degeneration with ubiquitin-positive inclusions Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontotemporal lobar degeneration with ubiquitin-positive inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

Parkinson disease 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson's disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson's disease 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.

Parkinson disease 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 18 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.

Parkinson disease 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 8, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

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

Parkinson disease 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 15 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.

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.

Parkinson disease 9 Gene Set

From CTD Gene-Disease Associations

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

Parkinson Disease Gene Set

From CTD Gene-Disease Associations

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

PARKINSON DISEASE 8, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 8, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease, Secondary Gene Set

From CTD Gene-Disease Associations

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

Parkinson Disease 3, Autosomal Dominant Lewy Body Gene Set

From CTD Gene-Disease Associations

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

PARKINSON DISEASE 5, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 5, AUTOSOMAL DOMINANT 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.

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.

Parkinson Disease 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 16 from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 12 from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 1, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 1, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 10 from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 4, Autosomal Dominant Lewy Body Gene Set

From CTD Gene-Disease Associations

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

PARKINSON DISEASE 11, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 11, AUTOSOMAL DOMINANT 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.

Parkinson Disease Gene Set

From dbGAP Gene-Trait Associations

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

parkinson's disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

parkinson's disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

secondary parkinson disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

parkinson's disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

postencephalitic parkinson disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

parkinson disease(c10.228.140.079.862.500)/genetics Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson disease(c10.228.140.079.862.500)/genetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease Gene Set

From GAD Gene-Disease Associations

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

parkinson's disease; depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease (familial) Gene Set

From GAD Gene-Disease Associations

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

parkinson's disease; hiv Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease; hiv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease; sleep disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

depression in parkinson's disease Gene Set

From GAD Gene-Disease Associations

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

parkinson's disease; cognition Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease; cognition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson's disease; alcohol abuse Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease; alcohol abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson 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.

myelodysplastic syndromes; parkinson disease; preleukemia Gene Set

From GAD Gene-Disease Associations

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

parkinson's disease; bipolar disorder Gene Set

From GAD Gene-Disease Associations

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

parkinson disease, essential tremor Gene Set

From GAD Gene-Disease Associations

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

gait ataxia; parkinson disease Gene Set

From GAD Gene-Disease Associations

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

parkinson's disease; hallucinations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinson's disease; hallucinations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Parkinson's disease (familial) Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Parkinson's disease (motor and cognition) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Parkinson's disease (motor and cognition) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Parkinson's disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Parkinson's disease 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.

parkinson's disease Gene Set

From GWASdb SNP-Disease Associations

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

Parkinson Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Parkinson Disease, Secondary Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Parkinson Disease, Secondary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype 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.

{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.

parkinson disease 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

{parkinson disease, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

parkinson disease 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 15, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 15, autosomal recessive 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.

{parkinson disease 16} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {parkinson disease 16} 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.

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.

?{parkinson disease 5, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?{parkinson disease 5, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease, juvenile, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease, juvenile, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Parkinson disease Gene Set

From PANTHER Pathways

proteins participating in the Parkinson disease pathway from the PANTHER Pathways dataset.

Parkinson's disease; ALS Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Parkinson's disease; ALS from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

synucleinopathy; Parkinson's disease Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease synucleinopathy; Parkinson's disease from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Parkinson's disease Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Parkinson's disease from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; addison's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; graves disease; graves' disease; hashimoto disease; polyendocrinopathies, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

central nervous system neoplasms; central nervous system tumors; glioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease central nervous system neoplasms; central nervous system tumors; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

central nervous system neoplasms; central nervous system tumors; lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease central nervous system neoplasms; central nervous system tumors; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cell transformation, neoplastic; central nervous system neoplasms; central nervous system tumors; lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; central nervous system neoplasms; central nervous system tumors; lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; diabetes, type 2; hypertension; cancer; depression; dementia; cerebrovascular disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; diabetes, type 2; hypertension; cancer; depression; dementia; cerebrovascular disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

dementia; disease progression Gene Set

From GAD Gene-Disease Associations

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

dementia; hallucinations; lewy body disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dementia; hallucinations; lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia in lewy body disease Gene Set

From GAD Gene-Disease Associations

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

aphasia; dementia; motor neuron disease; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aphasia; dementia; motor neuron disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; disease susceptibility Gene Set

From GAD Gene-Disease Associations

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

Alzheimer disease, familial, 3, with spastic paraparesis and apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis and apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer's disease Gene Set

From ClinVar Gene-Phenotype Associations

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

Alzheimer Disease 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 14 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 11 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 16 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 12 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 10 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 13 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 5 Gene Set

From CTD Gene-Disease Associations

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

Alzheimer Disease 6 Gene Set

From CTD Gene-Disease Associations

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

Alzheimer Disease Gene Set

From CTD Gene-Disease Associations

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

Alzheimer disease type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer disease type 4 from the curated CTD Gene-Disease Associations dataset.

Alzheimer disease type 2 Gene Set

From CTD Gene-Disease Associations

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

Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease 8 Gene Set

From CTD Gene-Disease Associations

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

Alzheimer Disease 9 Gene Set

From CTD Gene-Disease Associations

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

Alzheimer Disease 7 Gene Set

From CTD Gene-Disease Associations

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

Alzheimer Disease 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease 15 from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease Gene Set

From dbGAP Gene-Trait Associations

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

alzheimer's disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

alzheimer's disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

alzheimer's disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alzheimer's disease; depressive disorder, major Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; down syndrome Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; cerebrovascular disorders; Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; vascular endothelial growth factor levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; vascular endothelial growth factor levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; alzheimer's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; alzheimer's disease 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.

alzheimer's disease reduced Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; psychoses Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; atherosclerosis, coronary Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; anxiety disorder; depression; psychoses; aggressive behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; triglycerides; atherosclerosis, coronary Gene Set

From GAD Gene-Disease Associations

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

alzheimer`s disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; amnesia Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; abeta load in brain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; abeta load in brain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; abeta load Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; psychosis Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; essential tremor Gene Set

From GAD Gene-Disease Associations

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

neuropathy, alzheimer's disease related Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; atrophy; Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; als/amyotrophic lateral sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; als/amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; delusional disorder; aggressive behavior Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; asthma Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; aphasia; atrophy; syndrome Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; cognitive function Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; olfaction disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; type 2 diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; type 2 diabetes 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.

alzheimer disease; amnesia; atrophy; Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; down syndrome Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy 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.

alzheimer disease; psychomotor agitation Gene Set

From GAD Gene-Disease Associations

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

alzheimer's disease; aggressive behavior; psychotic symptoms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; aggressive behavior; psychotic symptoms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; schizophrenia Gene Set

From GAD Gene-Disease Associations

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

familial alzheimer's disease associated Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; cardiovascular diseases; colorectal neoplasms; macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; cardiovascular diseases; colorectal neoplasms; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; memory disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; cadaver Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; down syndrome; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; down syndrome; 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.

alzheimer's disease; aggressive behavior Gene Set

From GAD Gene-Disease Associations

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

Alzheimer's disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Alzheimer's disease 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.

Response to cholinesterase inhibitors in Alzheimer's disease Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to cholinesterase inhibitors in Alzheimer's disease 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.

Alzheimer's disease (cognitive decline) Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Alzheimer's disease biomarkers Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

alzheimer's disease Gene Set

From GWASdb SNP-Disease Associations

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

alzheimer disease Gene Set

From GWASdb SNP-Phenotype Associations

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

alzheimer disease Gene Set

From HPO Gene-Disease Associations

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

Alzheimer Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

alzheimer disease 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease-13} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease-13} 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.

{alzheimer disease-14} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease-14} phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease 18, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease 18, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease-7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease-7 phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease-5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease-5 phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease-4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease-4 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.

{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.

alzheimer disease 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease, type 3, with spastic paraparesis and unusual plaques Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease, type 3, with spastic paraparesis and unusual plaques phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

{alzheimer disease 16} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease 16} phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease-11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease-11 phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease-10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease-10 phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease 12} 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.

alzheimer disease 1, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease 1, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease-15} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {alzheimer disease-15} phenotype from the curated OMIM Gene-Disease Associations dataset.

alzheimer disease, type 3, with spastic paraparesis and apraxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the alzheimer disease, type 3, with spastic paraparesis and apraxia phenotype from the curated OMIM Gene-Disease Associations dataset.

{alzheimer disease, pathogenesis, association with} Gene Set

From OMIM Gene-Disease Associations

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

Alzheimer disease-amyloid secretase pathway Gene Set

From PANTHER Pathways

proteins participating in the Alzheimer disease-amyloid secretase pathway pathway from the PANTHER Pathways dataset.

Alzheimer disease-presenilin pathway Gene Set

From PANTHER Pathways

proteins participating in the Alzheimer disease-presenilin pathway pathway from the PANTHER Pathways dataset.

alzheimer disease specific cell type Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue alzheimer disease specific cell type in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

type 2 diabetes; Alzheimer's disease Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease type 2 diabetes; Alzheimer's disease from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Alzheimer's disease Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Alzheimer's disease from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Alzheimer's disease; FTLD Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Alzheimer's disease; FTLD from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Alzheimer's disease; ALS Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Alzheimer's disease; ALS from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Alzheimer's disease; schizophrenia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Alzheimer's disease; schizophrenia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Cerebral palsy, spastic quadriplegic, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral palsy, spastic quadriplegic, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral palsy, spastic quadriplegic, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

From CTD Gene-Disease Associations

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

Cerebral Palsy, Ataxic, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Ataxic, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy, Spastic Quadriplegic, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 2 from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy Gene Set

From CTD Gene-Disease Associations

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

Cerebral Palsy, Spastic Quadriplegic, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Spastic Quadriplegic, 1 from the curated CTD Gene-Disease Associations dataset.

cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bell's palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

partial third-nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ataxic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fourth cranial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cranial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pseudobulbar palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spastic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dyskinetic cerebral palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tibial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

conjugate gaze palsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cerebral palsy Gene Set

From GAD Gene-Disease Associations

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

cerebral palsy; hemiplegia Gene Set

From GAD Gene-Disease Associations

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

cerebral palsy; Gene Set

From GAD Gene-Disease Associations

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

cerebral palsy; hemiplegia; virus diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral palsy; hemiplegia; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral palsy; pregnancy complications, infectious; virus diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral palsy; pregnancy complications, infectious; virus diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cerebral palsy; intracranial thrombosis; obstetric labor complications; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vocal cord palsy Gene Set

From GAD Gene-Disease Associations

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

palsy Gene Set

From GeneRIF Biological Term Annotations

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

cerebral palsy Gene Set

From HPO Gene-Disease Associations

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

facial palsy Gene Set

From HPO Gene-Disease Associations

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

paraganglioma-related cranial nerve palsy Gene Set

From HPO Gene-Disease Associations

genes associated with the paraganglioma-related cranial nerve palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abducens palsy Gene Set

From HPO Gene-Disease Associations

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

facial palsy secondary to cranial hyperostosis Gene Set

From HPO Gene-Disease Associations

genes associated with the facial palsy secondary to cranial hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bulbar palsy Gene Set

From HPO Gene-Disease Associations

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

oculomotor nerve palsy Gene Set

From HPO Gene-Disease Associations

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

Cerebral Palsy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

cerebral palsy, spastic quadriplegic, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral palsy, spastic quadriplegic, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral palsy, spastic quadriplegic, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral palsy, spastic quadriplegic, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic progressive chorea; huntington disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic progressive chorea; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic progressive chorea; huntington disease; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic progressive chorea; huntington disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Wolff-Parkinson-White Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wolff-Parkinson-White Syndrome from the curated CTD Gene-Disease Associations dataset.

wolff-parkinson-white syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease wolff-parkinson-white syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

wolff-parkinson-white syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

parkinson Gene Set

From GeneRIF Biological Term Annotations

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

Parkinson's Disease_Substantia Nigra_GSE7621 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Parkinson's Disease_Substantia Nigra_GSE7621 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

wolff-parkinson-white syndrome Gene Set

From HPO Gene-Disease Associations

genes associated with the wolff-parkinson-white syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Wolff-Parkinson-White Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Wolff-Parkinson-White Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

wolff-parkinson-white syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the wolff-parkinson-white syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson's Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Congenital heart disease, multiple types, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.

Multiple Sulfatase Deficiency Disease Gene Set

From CTD Gene-Disease Associations

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

crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic predisposition to disease; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic predisposition to disease; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene Set

From GAD Gene-Disease Associations

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

head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; leukemia; multiple myeloma; recurrence Gene Set

From GAD Gene-Disease Associations

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

{vitiligo-associated multiple autoimmune disease susceptiblity 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {vitiligo-associated multiple autoimmune disease susceptiblity 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, disease progression, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, disease progression, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

{vitiligo-associated multiple autoimmune disease susceptibility 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {vitiligo-associated multiple autoimmune disease susceptibility 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

Dementia familial British Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dementia familial British phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dementia, familial Danish Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dementia, familial Danish phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lewy body dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lewy body dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dementia Gene Set

From CTD Gene-Disease Associations

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

Dementia, familial British Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dementia, familial British from the curated CTD Gene-Disease Associations dataset.

Dementia, familial Danish Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dementia, familial Danish from the curated CTD Gene-Disease Associations dataset.

Delirium, Dementia, Amnestic, Cognitive Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Delirium, Dementia, Amnestic, Cognitive Disorders from the curated CTD Gene-Disease Associations dataset.

Dementia, Vascular Gene Set

From CTD Gene-Disease Associations

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

AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1 from the curated CTD Gene-Disease Associations dataset.

dementia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

dementia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

vascular dementia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

dementia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vascular dementia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

lewy body dementia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain injuries; dementia, vascular; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain injuries; dementia, vascular; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia, multi-infarct Gene Set

From GAD Gene-Disease Associations

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

cerebrovascular disorders; dementia Gene Set

From GAD Gene-Disease Associations

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

cerebral hemorrhage; cerebral hemorrhages; dementia, vascular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; dementia, vascular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inherited dementia ftdp-17 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inherited dementia ftdp-17 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; memory disorders; stroke Gene Set

From GAD Gene-Disease Associations

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

dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

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

dementia, vascular; Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; dementia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia in other conditions Gene Set

From GAD Gene-Disease Associations

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

dementia; als/amyotrophic lateral sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dementia; als/amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; hyperhomocysteinemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

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

dementia; hyperlipidemias Gene Set

From GAD Gene-Disease Associations

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

atrophy; dementia Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; dementia; diabetes mellitus; hypercholesterolemia; pancreatitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; dementia; diabetes mellitus; hypercholesterolemia; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv infection; dementia, aids Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infection; dementia, aids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia, vascular; vascular diseases Gene Set

From GAD Gene-Disease Associations

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

dementia but not cardiovascular mortality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dementia but not cardiovascular mortality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia, vascular; inflammation; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dementia, vascular; inflammation; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; down syndrome Gene Set

From GAD Gene-Disease Associations

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

stroke; dementia Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; dementia; parkinsonian disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; dementia; parkinsonian disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyotrophic lateral sclerosis; dementia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain ischemia; dementia; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; dementia; hypoalphalipoproteinemias; intracranial arteriosclerosis; intracranial thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; tauopathies Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; dementia Gene Set

From GAD Gene-Disease Associations

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

vascular dementia Gene Set

From GAD Gene-Disease Associations

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

hereditary dementia. Gene Set

From GAD Gene-Disease Associations

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

apoplexy; brain ischemia; dementia, vascular; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; dementia, vascular; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia Gene Set

From GAD Gene-Disease Associations

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

dementia; Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; dementia Gene Set

From GAD Gene-Disease Associations

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

dementia; diseases in twins Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; dementia; diabetes mellitus type ii; diabetes mellitus, type 2; obesity Gene Set

From GAD Gene-Disease Associations

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

dementia; neuropathy Gene Set

From GAD Gene-Disease Associations

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

apoplexy; dementia; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; dementia; myocardial infarction; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; olfaction disorders Gene Set

From GAD Gene-Disease Associations

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

brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain infarction; cerebral amyloid angiopathy; dementia; diabetes mellitus; hyperinsulinism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aids dementia complex; hiv infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids dementia complex; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia, vascular Gene Set

From GAD Gene-Disease Associations

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

dementia; diabetes complications Gene Set

From GAD Gene-Disease Associations

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

dementia; inflammation Gene Set

From GAD Gene-Disease Associations

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

dementia; neurodegenerative diseases; prion diseases Gene Set

From GAD Gene-Disease Associations

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

brain injuries; dementia Gene Set

From GAD Gene-Disease Associations

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

dementia Gene Set

From GeneRIF Biological Term Annotations

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

HIV-associated dementia Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Vascular dementia Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

dementia Gene Set

From GWASdb SNP-Disease Associations

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

vascular dementia Gene Set

From GWASdb SNP-Disease Associations

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

dementia Gene Set

From GWASdb SNP-Phenotype Associations

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

frontolimbic dementia Gene Set

From HPO Gene-Disease Associations

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

subcortical dementia Gene Set

From HPO Gene-Disease Associations

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

dementia Gene Set

From HPO Gene-Disease Associations

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

frontal lobe dementia Gene Set

From HPO Gene-Disease Associations

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

Dementia, Multi-Infarct Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

AIDS Dementia Complex Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Dementia, Vascular Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Delirium, Dementia, Amnestic, Cognitive Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Delirium, Dementia, Amnestic, Cognitive Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Dementia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

{lewy body dementia, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {lewy body dementia, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, familial danish Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, familial danish phenotype from the curated OMIM Gene-Disease Associations dataset.

{dementia, vascular, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

dementia, familial, nonspecific Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, familial, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, familial british Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, familial british phenotype from the curated OMIM Gene-Disease Associations dataset.

{amyotrophic lateral sclerosis-parkinsonism/dementia complex, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {amyotrophic lateral sclerosis-parkinsonism/dementia complex, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, lewy body Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, lewy body phenotype from the curated OMIM Gene-Disease Associations dataset.

neoplasms ; osteoporosis; alzheimer diseasey; cardiovascular diseases; metabolic syndrome x; diabetes complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms ; osteoporosis; alzheimer diseasey; cardiovascular diseases; metabolic syndrome x; diabetes complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer Gene Set

From GeneRIF Biological Term Annotations

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

Alzheimer's Disease_CNS - Brain - Hippocampus (MMHCC)_GSE1297 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Alzheimer's Disease_CNS - Brain - Hippocampus (MMHCC)_GSE1297 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Alzheimer's Disease_Entorhinal cortex_GSE5281 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Alzheimer's Disease_Entorhinal cortex_GSE5281 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

alzheimer's Gene Set

From Phosphosite Textmining Biological Term Annotations

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

integumentary system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

reproductive system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

autoimmune disease of endocrine system Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease autoimmune disease of endocrine system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

gastrointestinal system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

female reproductive system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

central nervous system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

immune system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

respiratory system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hematopoietic system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

autoimmune disease of the nervous system Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease autoimmune disease of the nervous system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

nervous system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

autoimmune disease of central nervous system Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease autoimmune disease of central nervous system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

endocrine system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

auditory system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

musculoskeletal system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

male reproductive system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

cardiovascular system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

sensory system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

lymphatic system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

autoimmune disease of cardiovascular system Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease autoimmune disease of cardiovascular system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of peripheral nervous system Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease autoimmune disease of peripheral nervous system from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

peripheral nervous system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

urinary system disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

immune system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

reproductive system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

cardiovascular system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

gastrointestinal system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

central nervous system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

integumentary system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

respiratory system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

hematopoietic system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

nervous system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

endocrine system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

auditory system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

musculoskeletal system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

male reproductive system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

sensory system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

lymphatic system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

female reproductive system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

urinary system disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

reproductive system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

immune system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

nervous system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

endocrine system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

musculoskeletal system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autoimmune disease of peripheral nervous system Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

peripheral nervous system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

respiratory system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cardiovascular system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central nervous system hereditary degenerative disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease central nervous system hereditary degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sensory system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

lymphatic system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autoimmune disease of cardiovascular system Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

auditory system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autoimmune disease of endocrine system Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

female reproductive system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

integumentary system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autoimmune disease of central nervous system Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autoimmune disease of the nervous system Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autonomic nervous system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

male reproductive system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gastrointestinal system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central nervous system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hematopoietic system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

urinary system disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autoimmune diseases; celiac disease; diabetes mellitus, type 1; endocrine system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; celiac disease; diabetes mellitus, type 1; endocrine system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; iatrogenic disease; peripheral nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; iatrogenic disease; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digestive system abnormalities; hirschsprung disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digestive system abnormalities; hirschsprung disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemochromatosis; hiv infections; peripheral nervous system diseases; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; hiv infections; peripheral nervous system diseases; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; demyelinating diseases; peripheral nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

reproductive system disease Gene Set

From GWASdb SNP-Disease Associations

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

cardiovascular system disease Gene Set

From GWASdb SNP-Disease Associations

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

autoimmune disease of endocrine system Gene Set

From GWASdb SNP-Disease Associations

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

gastrointestinal system disease Gene Set

From GWASdb SNP-Disease Associations

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

central nervous system disease Gene Set

From GWASdb SNP-Disease Associations

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

integumentary system disease Gene Set

From GWASdb SNP-Disease Associations

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

immune system disease Gene Set

From GWASdb SNP-Disease Associations

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

respiratory system disease Gene Set

From GWASdb SNP-Disease Associations

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

hematopoietic system disease Gene Set

From GWASdb SNP-Disease Associations

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

autoimmune disease of the nervous system Gene Set

From GWASdb SNP-Disease Associations

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

nervous system disease Gene Set

From GWASdb SNP-Disease Associations

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

endocrine system disease Gene Set

From GWASdb SNP-Disease Associations

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

auditory system disease Gene Set

From GWASdb SNP-Disease Associations

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

musculoskeletal system disease Gene Set

From GWASdb SNP-Disease Associations

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

male reproductive system disease Gene Set

From GWASdb SNP-Disease Associations

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

sensory system disease Gene Set

From GWASdb SNP-Disease Associations

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

lymphatic system disease Gene Set

From GWASdb SNP-Disease Associations

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

female reproductive system disease Gene Set

From GWASdb SNP-Disease Associations

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

urinary system disease Gene Set

From GWASdb SNP-Disease Associations

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

Epilepsy, progressive myoclonic 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy, progressive, with ovarian failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy, progressive, with ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive pseudorheumatoid dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperpigmentation, familial progressive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Progressive intrahepatic cholestasis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial heart block type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial heart block type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 2b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive familial intrahepatic cholestasis 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive myoclonus epilepsy with ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive myoclonus epilepsy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive sclerosing poliodystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis with progressive nerve deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis with progressive nerve deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive myositis ossificans Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive myositis ossificans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoclonic Epilepsies, Progressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myoclonic Epilepsies, Progressive from the curated CTD Gene-Disease Associations dataset.

Cataract, Nuclear Progressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Nuclear Progressive from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset.

Gliosis, Familial Progressive Subcortical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.

HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.

Osseous Heteroplasia, Progressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osseous Heteroplasia, Progressive from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Progressive Myoclonic, 1b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Progressive Myoclonic, 1b from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.

Chorioretinal atrophy, progressive bifocal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset.

Macrothrombocytopenia progressive deafness Gene Set

From CTD Gene-Disease Associations

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

Erythrokeratodermia, Progressive Symmetric Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Erythrokeratodermia, Progressive Symmetric from the curated CTD Gene-Disease Associations dataset.

Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset.

Progressive hearing loss stapes fixation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive hearing loss stapes fixation from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.

PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA 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.

Leukoencephalopathy, Progressive Multifocal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy, Progressive Multifocal from the curated CTD Gene-Disease Associations dataset.

Progressive Familial Heart Block, Type Ib Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.

Cholestasis, progressive familial intrahepatic 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.

Ophthalmoplegia, Chronic Progressive External Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ophthalmoplegia, Chronic Progressive External from the curated CTD Gene-Disease Associations dataset.

Nephropathy, Progressive, with Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephropathy, Progressive, with Deafness from the curated CTD Gene-Disease Associations dataset.

Renal Failure, Progressive, with Hypertension Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Failure, Progressive, with Hypertension from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 from the curated CTD Gene-Disease Associations dataset.

chronic progressive external ophthalmoplegia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

progressive myoclonus epilepsy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

chronic progressive external ophthalmoplegia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

progressive multifocal leukoencephalopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

rapidly progressive glomerulonephritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

progressive muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

progressive myoclonus epilepsy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

slowly progressive als Gene Set

From GAD Gene-Disease Associations

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

ophthalmoplegia, chronic progressive external Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ophthalmoplegia, chronic progressive external in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

primary progressive aphasia Gene Set

From GAD Gene-Disease Associations

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

chronic progressive chorea; Gene Set

From GAD Gene-Disease Associations

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

dominant progressive deafness Gene Set

From GAD Gene-Disease Associations

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

rapidly progressive familial amyotrophic lateral sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

progressive av-block and anomalous venous return Gene Set

From GAD Gene-Disease Associations

genes associated with the disease progressive av-block and anomalous venous return in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

progressive external ophthalmoplegia Gene Set

From GAD Gene-Disease Associations

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

als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

progressive renal damage Gene Set

From GAD Gene-Disease Associations

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

chronic progressive chorea; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic progressive chorea; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

progressive Gene Set

From GeneRIF Biological Term Annotations

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

progressive cataract Gene Set

From HPO Gene-Disease Associations

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

progressive inability to walk Gene Set

From HPO Gene-Disease Associations

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

progressive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

progressive congenital scoliosis Gene Set

From HPO Gene-Disease Associations

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

progressive visual field defects Gene Set

From HPO Gene-Disease Associations

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

symmetrical progressive peripheral demyelination Gene Set

From HPO Gene-Disease Associations

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

progressive spastic paraplegia Gene Set

From HPO Gene-Disease Associations

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

progressive cone degeneration Gene Set

From HPO Gene-Disease Associations

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

progressive vitiligo Gene Set

From HPO Gene-Disease Associations

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

progressive neurologic deterioration Gene Set

From HPO Gene-Disease Associations

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

progressive spastic quadriplegia Gene Set

From HPO Gene-Disease Associations

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

progressive psychomotor deterioration Gene Set

From HPO Gene-Disease Associations

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

progressive reticulate hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

progressive fusion 2nd-5th pip joints Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive fusion 2nd-5th pip joints 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.

progressive extrapyramidal movement disorder Gene Set

From HPO Gene-Disease Associations

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

progressive gait ataxia Gene Set

From HPO Gene-Disease Associations

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

progressive inspiratory stridor Gene Set

From HPO Gene-Disease Associations

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

progressive choreoathetosis Gene Set

From HPO Gene-Disease Associations

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

progressive spasticity Gene Set

From HPO Gene-Disease Associations

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

progressive peripheral neuropathy Gene Set

From HPO Gene-Disease Associations

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

progressive sclerosis of skull base Gene Set

From HPO Gene-Disease Associations

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

progressive clavicular acroosteolysis Gene Set

From HPO Gene-Disease Associations

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

progressive muscle weakness Gene Set

From HPO Gene-Disease Associations

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

progressive alopecia Gene Set

From HPO Gene-Disease Associations

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

progressive distal muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

progressive truncal ataxia Gene Set

From HPO Gene-Disease Associations

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

subacute progressive viral hepatitis Gene Set

From HPO Gene-Disease Associations

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

intellectual disability, progressive Gene Set

From HPO Gene-Disease Associations

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

progressive central visual loss Gene Set

From HPO Gene-Disease Associations

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

progressive language deterioration Gene Set

From HPO Gene-Disease Associations

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

progressive hyperpigmentation Gene Set

From HPO Gene-Disease Associations

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

progressive hypotrichosis Gene Set

From HPO Gene-Disease Associations

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

progressive sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

progressive pulmonary function impairment Gene Set

From HPO Gene-Disease Associations

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

progressive forgetfulness Gene Set

From HPO Gene-Disease Associations

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

progressive microcephaly Gene Set

From HPO Gene-Disease Associations

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

progressive alveolar ridge hypertropy Gene Set

From HPO Gene-Disease Associations

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

progressive proximal muscle weakness Gene Set

From HPO Gene-Disease Associations

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

progressive macrocephaly Gene Set

From HPO Gene-Disease Associations

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

progressive external ophthalmoplegia Gene Set

From HPO Gene-Disease Associations

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

progressive night blindness Gene Set

From HPO Gene-Disease Associations

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

progressive macular scarring Gene Set

From HPO Gene-Disease Associations

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

progressive ptosis Gene Set

From HPO Gene-Disease Associations

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

progressive calcification of costochondral cartilage Gene Set

From HPO Gene-Disease Associations

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

progressive cervical vertebral spine fusion Gene Set

From HPO Gene-Disease Associations

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

progressive conductive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

progressive distal muscle weakness Gene Set

From HPO Gene-Disease Associations

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

rapidly progressive Gene Set

From HPO Gene-Disease Associations

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

progressive leukoencephalopathy Gene Set

From HPO Gene-Disease Associations

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

progressive retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

progressive flexion contractures Gene Set

From HPO Gene-Disease Associations

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

progressive visual loss Gene Set

From HPO Gene-Disease Associations

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

progressive disorder Gene Set

From HPO Gene-Disease Associations

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

progressive ophthalmoplegia Gene Set

From HPO Gene-Disease Associations

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

progressive cerebellar ataxia Gene Set

From HPO Gene-Disease Associations

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

Myoclonic Epilepsies, Progressive Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Aphasia, Primary Progressive Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Ophthalmoplegia, Chronic Progressive External Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ophthalmoplegia, Chronic Progressive External phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Progressive rod-cone degeneration protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Progressive rod-cone degeneration protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Progressive ankylosis Gene Set

From InterPro Predicted Protein Domain Annotations

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

progressive muscle weakness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

progressive hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the progressive hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

deafness, x-linked 1, progressive Gene Set

From OMIM Gene-Disease Associations

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

epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive canalicular Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive canalicular phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 2b (lafora) Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 2b (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia, autosomal dominant, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia, autosomal dominant, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive familial heart block, type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

macrothrombocytopenia and progressive sensorineural deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrothrombocytopenia and progressive sensorineural deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy with progressive myoclonic epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperpigmentation, familial progressive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive familial intrahepatic 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive familial intrahepatic 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive familial intrahepatic 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cholestasis, progressive familial intrahepatic 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cholestasis, progressive familial intrahepatic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

aphasia, primary progressive Gene Set

From OMIM Gene-Disease Associations

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

spondyloepiphyseal dysplasia tarda with progressive arthropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia tarda with progressive arthropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy, progressive x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy, progressive, with ovarian failure Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy, progressive, with ovarian failure phenotype from the curated OMIM Gene-Disease Associations dataset.

osseous heteroplasia, progressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the osseous heteroplasia, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.

nephropathy, progressive, with deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephropathy, progressive, with deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia, autosomal dominant 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.

progressive external ophthalmoplegia with mitochondrial dna deletions 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions 3 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.

cataract 27, nuclear progressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 27, nuclear progressive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

progressive external ophthalmoplegia, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the progressive external ophthalmoplegia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

heart block, progressive, type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the heart block, progressive, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 1a (unverricht and lundborg) Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 1a (unverricht and lundborg) phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 2a (lafora) Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 2a (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.

Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set

From Reactome Pathways

proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways dataset.

coronary artery disease; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; coronary artery disease; crohn disease; crohn's disease; diabetes mellitus; hypertension; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

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

activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; granuloma; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; crohn disease; crohn's disease; diabetes mellitus; disease; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

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

addison disease; graves disease; hashimoto disease Gene Set

From GAD Gene-Disease Associations

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

crohn disease; crohn's disease; disease susceptibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; disease susceptibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; colorectal neoplasms; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; disease susceptibility; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graves disease; graves' disease; hashimoto disease; hypothyroidism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graves disease; graves' disease; hashimoto disease; hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; graves disease; graves' disease; hashimoto disease; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colitis; crohn disease; crohn's disease; disease models, animal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis; crohn disease; crohn's disease; disease models, animal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammation; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary disease; coronary heart disease; graft vs host disease Gene Set

From GAD Gene-Disease Associations

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

multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation Gene Set

From Biocarta Pathways

proteins participating in the multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation pathway from the Biocarta Pathways dataset.

CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN Gene Set

From CHEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Multiple synostoses syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract 15, multiple types Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract 15, multiple types phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, autosomal dominant, multiple types, with microcornea Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal multiple pterygium syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous and Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia with multiple dislocations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia with multiple dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple endocrine neoplasia, type 2b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple endocrine neoplasia, type 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple fibrofolliculomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple fibrofolliculomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple synostoses syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple synostoses syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple pterygium syndrome Escobar type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple gastrointestinal atresias Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple gastrointestinal atresias phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple exostoses type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple exostoses type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple endocrine neoplasia, type 2a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple mitochondrial dysfunctions syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple mitochondrial dysfunctions syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial multiple polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple endocrine neoplasia, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple endocrine neoplasia, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital exostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple fibroadenomas of the breast Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple fibroadenomas of the breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LIPOMATOSIS, MULTIPLE Gene Set

From CTD Gene-Disease Associations

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

Multiple Endocrine Neoplasia Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.

Cafe au lait spots, multiple Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cafe au lait spots, multiple from the curated CTD Gene-Disease Associations dataset.

Multiple Organ Failure Gene Set

From CTD Gene-Disease Associations

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

EXOSTOSES, MULTIPLE, TYPE II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE II from the curated CTD Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia Type 2a Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2a from the curated CTD Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

Multiple Myeloma Gene Set

From CTD Gene-Disease Associations

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

Venous Malformations, Multiple Cutaneous and Mucosal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset.

Multiple Synostoses Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Synostoses Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

CATARACT 32, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 32, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Exostoses, Multiple Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exostoses, Multiple Hereditary from the curated CTD Gene-Disease Associations dataset.

Hamartoma Syndrome, Multiple Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hamartoma Syndrome, Multiple from the curated CTD Gene-Disease Associations dataset.

Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.

CATARACT 6, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 6, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia Gene Set

From CTD Gene-Disease Associations

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

Exostoses, Multiple, Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exostoses, Multiple, Type III from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Multiple Sclerosis Gene Set

From CTD Gene-Disease Associations

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

Multiple Chemical Sensitivity Gene Set

From CTD Gene-Disease Associations

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

Multiple synostoses syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple synostoses syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Multiple Sclerosis, Relapsing-Remitting Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Sclerosis, Relapsing-Remitting from the curated CTD Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia Type 2b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2b from the curated CTD Gene-Disease Associations dataset.

MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Dominant, Multiple Types 1 Gene Set

From CTD Gene-Disease Associations

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

Trichoepithelioma multiple familial Gene Set

From CTD Gene-Disease Associations

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

Multiple pterygium syndrome Gene Set

From CTD Gene-Disease Associations

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

Abnormalities, Multiple Gene Set

From CTD Gene-Disease Associations

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

Multiple Endocrine Neoplasia, Type IV Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia, Type IV from the curated CTD Gene-Disease Associations dataset.

CATARACT 3, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 3, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset.

EXOSTOSES, MULTIPLE, TYPE I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE I from the curated CTD Gene-Disease Associations dataset.

CATARACT 4, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 4, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

MULTIPLE SYNOSTOSES SYNDROME 1 Gene Set