Name

multiple sclerosis; optic neuritis Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence 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.

optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Optic Neuritis Gene Set

From CTD Gene-Disease Associations

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

optic neuritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retrobulbar optic neuritis Gene Set

From HPO Gene-Disease Associations

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

optic neuritis Gene Set

From HPO Gene-Disease Associations

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

Optic Neuritis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

multiple sclerosis(ppmultiple sclerosis) Gene Set

From GAD Gene-Disease Associations

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

Multiple sclerosis or amyotrophic lateral sclerosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis or amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Neuritis Gene Set

From CTD Gene-Disease Associations

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

Brachial Plexus Neuritis Gene Set

From CTD Gene-Disease Associations

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

neuritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brachial plexus neuritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

motor neuritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hiv infections; neuritis; somatosensory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv infections; neuritis; somatosensory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuritis Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term neuritis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations 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 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 Sclerosis Gene Set

From dbGAP Gene-Trait Associations

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

multiple sclerosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

multiple sclerosis Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

relapsing-remitting multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD 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.

autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis (age of onset) Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; diabetes, type 1 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.

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.

susceptibility to multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

learning disorders; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis; lupus erythematosus Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis Gene Set

From GAD Gene-Disease Associations

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

apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke 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.

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.

encephalomyelitis, autoimmune, experimental; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease encephalomyelitis, autoimmune, experimental; multiple sclerosis 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.

multiple sclerosis; neuromyelitis optica Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis, relapsing-remitting; recurrence Gene Set

From GAD Gene-Disease Associations

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

normalized brain volume, multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

lupus erythematosus, systemic; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis; recurrence Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis; iga nephropathy Gene Set

From GAD Gene-Disease Associations

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

churg-strauss syndrome; multiple sclerosis; wegener granulomatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease churg-strauss syndrome; multiple sclerosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile multiple sclerosis 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.

diabetes mellitus, type 1; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

hepatitis c, chronic; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

atrophy; multiple sclerosis, relapsing-remitting Gene Set

From GAD Gene-Disease Associations

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

multiple sclerosis (severity) Gene Set

From GAD Gene-Disease Associations

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

epstein-barr virus infections; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epstein-barr virus infections; multiple sclerosis 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.

multiple sclerosis, relapsing-remitting Gene Set

From GAD Gene-Disease Associations

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

malaria, falciparum; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

early onset of multiple sclerosis. Gene Set

From GAD Gene-Disease Associations

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

breast neoplasms; carcinoma; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

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

MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Multiple sclerosis--Brain Glutamate Levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis--Brain Glutamate Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Multiple sclerosis (severity) Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Multiple sclerosis (OCB status) Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Multiple sclerosis (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

multiple sclerosis Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GWASdb SNP-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.

Multiple Sclerosis, Relapsing-Remitting Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Multiple Sclerosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

{multiple sclerosis, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

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

{multiple sclerosis, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, susceptibility to, 4} 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.

{multiple sclerosis, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

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

{multiple sclerosis, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, susceptibility to, 3} phenotype from the curated OMIM 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.

lateral terminal nucleus of the accessory optic tract, lateral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral terminal nucleus of the accessory optic tract, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral terminal nucleus of the accessory optic tract, ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral terminal nucleus of the accessory optic tract, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

dorsal terminal nucleus of the accessory optic tract Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in dorsal terminal nucleus of the accessory optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, optic layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, optic layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Nucleus of the optic tract Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Nucleus of the optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Lateral terminal nucleus of the accessory optic tract Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Lateral terminal nucleus of the accessory optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

optic fiber layer of SC Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in optic fiber layer of SC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bosch-boonstra-schaaf optic atrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dominant hereditary optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic Atrophy Type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma of optic disc Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma of optic disc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic nerve hypoplasia, bilateral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic nerve hypoplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic nerve aplasia, bilateral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic nerve aplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Septo-optic dysplasia sequence Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Septo-optic dysplasia sequence phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy, Hereditary, Leber Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 1 and deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy 7 Gene Set

From CTD Gene-Disease Associations

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

Optic Atrophy 4 Gene Set

From CTD Gene-Disease Associations

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

Optic atrophy 5 Gene Set

From CTD Gene-Disease Associations

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

Optic Atrophies, Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophies, Hereditary from the curated CTD Gene-Disease Associations dataset.

Optic Nerve Hypoplasia, Bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Nerve Hypoplasia, Bilateral from the curated CTD Gene-Disease Associations dataset.

Polymicrogyria With Optic Nerve Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polymicrogyria With Optic Nerve Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Costeff optic atrophy syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset.

Optic atrophy polyneuropathy deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 6 Gene Set

From CTD Gene-Disease Associations

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

Optic atrophy and cataract, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Optic Nerve Diseases Gene Set

From CTD Gene-Disease Associations

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

Cavitary Optic Disc Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cavitary Optic Disc Anomalies from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy Gene Set

From CTD Gene-Disease Associations

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

Coloboma of optic nerve Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coloboma of optic nerve from the curated CTD Gene-Disease Associations dataset.

OPTIC ATROPHY 2 Gene Set

From CTD Gene-Disease Associations

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

Optic Neuropathy, Ischemic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Neuropathy, Ischemic from the curated CTD Gene-Disease Associations dataset.

Optic Atrophy, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Optic Disk Gene Set

From dbGAP Gene-Trait Associations

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

Optic Nerve Gene Set

From dbGAP Gene-Trait Associations

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

toxic optic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic nerve disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

primary optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic nerve neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic papillitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

leber hereditary optic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic disk drusen Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

anterior ischemic optic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic nerve sheath meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic nerve glioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

partial optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

optic atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leber's hereditary optic neuropathy Gene Set

From GAD Gene-Disease Associations

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

optic disc atrophy Gene Set

From GAD Gene-Disease Associations

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

optic atrophy Gene Set

From GAD Gene-Disease Associations

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

optic nerve diseases Gene Set

From GAD Gene-Disease Associations

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

blindness; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic disk Gene Set

From GAD Gene-Disease Associations

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

optic nerve Gene Set

From GAD Gene-Disease Associations

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

cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

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

optic atrophy, hereditary, leber; vision disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic nerve malformation Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; optic neuropathy, ischemic Gene Set

From GAD Gene-Disease Associations

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

optic atrophy and moderate deafness Gene Set

From GAD Gene-Disease Associations

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

optic Gene Set

From GeneRIF Biological Term Annotations

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

optic nerve development Gene Set

From GO Biological Process Annotations

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

optic nerve morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the optic nerve morphogenesis biological process from the curated GO Biological Process Annotations dataset.

optic vesicle morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the optic vesicle morphogenesis biological process from the curated GO Biological Process Annotations dataset.

optic placode formation Gene Set

From GO Biological Process Annotations

genes participating in the optic placode formation biological process from the curated GO Biological Process Annotations dataset.

optic cup morphogenesis involved in camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

positive regulation of optic nerve formation Gene Set

From GO Biological Process Annotations

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

regulation of optic nerve formation Gene Set

From GO Biological Process Annotations

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

optic cup structural organization Gene Set

From GO Biological Process Annotations

genes participating in the optic cup structural organization biological process from the curated GO Biological Process Annotations dataset.

optic nerve structural organization Gene Set

From GO Biological Process Annotations

genes participating in the optic nerve structural organization biological process from the curated GO Biological Process Annotations dataset.

closure of optic fissure Gene Set

From GO Biological Process Annotations

genes participating in the closure of optic fissure biological process from the curated GO Biological Process Annotations dataset.

optic cup formation involved in camera-type eye development Gene Set

From GO Biological Process Annotations

genes participating in the optic cup formation involved in camera-type eye development biological process from the curated GO Biological Process Annotations dataset.

optic placode formation involved in camera-type eye formation Gene Set

From GO Biological Process Annotations

genes participating in the optic placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations dataset.

optic chiasma development Gene Set

From GO Biological Process Annotations

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

Optic nerve measurement (rim area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (rim area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (cup area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (cup area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (disc area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (disc area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (cup-to-disc ratio) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (cup-to-disc ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic disc parameters Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic disc parameters phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

optic nerve disease Gene Set

From GWASdb SNP-Disease Associations

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

optic nerve coloboma Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the optic nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic disc hypoplasia Gene Set

From HPO Gene-Disease Associations

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

optic neuropathy Gene Set

From HPO Gene-Disease Associations

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

optic atrophy Gene Set

From HPO Gene-Disease Associations

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

optic disc drusen Gene Set

From HPO Gene-Disease Associations

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

abnormality of the optic disc Gene Set

From HPO Gene-Disease Associations

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

optic disc pallor Gene Set

From HPO Gene-Disease Associations

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

leber optic atrophy Gene Set

From HPO Gene-Disease Associations

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

optic atrophy from cranial nerve compression Gene Set

From HPO Gene-Disease Associations

genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic nerve dysplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the optic tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nonarteritic anterior ischemic optic neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the nonarteritic anterior ischemic optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the optic tract Gene Set

From HPO Gene-Disease Associations

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

optic nerve compression Gene Set

From HPO Gene-Disease Associations

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

optic nerve hypoplasia Gene Set

From HPO Gene-Disease Associations

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

septo-optic dysplasia Gene Set

From HPO Gene-Disease Associations

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

optic glioma Gene Set

From HPO Gene-Disease Associations

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

abnormality of the optic nerve Gene Set

From HPO Gene-Disease Associations

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

Septo-Optic Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Optic Atrophies, Hereditary Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Optic Nerve Glioma Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Optic Disk Drusen Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Optic Atrophy, Hereditary, Leber Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Atrophy, Autosomal Dominant Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Optic Nerve Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Optic Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Optic Neuropathy, Ischemic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Optic atrophy 3-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal optic disc morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic stalk morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent optic tract Gene Set

From MPO Gene-Phenotype Associations

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

optic nerve degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent optic placodes Gene Set

From MPO Gene-Phenotype Associations

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

optic nerve coloboma Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic tract morphology Gene Set

From MPO Gene-Phenotype Associations

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

optic neuropathy Gene Set

From MPO Gene-Phenotype Associations

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

optic nerve atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic placode morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic nerve innervation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal optic nerve innervation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent optic nerve Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic nerve morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic cup morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic chiasm morphology Gene Set

From MPO Gene-Phenotype Associations

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

optic nerve swelling Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve swelling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic vesicle formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal optic vesicle formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic fissure morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent optic vesicle Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic fissure closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

optic nerve cupping Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve cupping phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent optic disc Gene Set

From MPO Gene-Phenotype Associations

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

delayed optic fissure closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged optic nerve Gene Set

From MPO Gene-Phenotype Associations

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

optic disc coloboma Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic disc coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic choroid morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic eminence morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent optic chiasm Gene Set

From MPO Gene-Phenotype Associations

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

optic nerve hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic pit morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic canal morphology Gene Set

From MPO Gene-Phenotype Associations

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

optic atrophy 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy-4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.

foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

optic nerve hypoplasia and abnormalities of the central nervous system Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy-7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset.

cavitary optic disc anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the cavitary optic disc anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia, optic atrophy, and neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

bosch-boonstra-schaaf optic atrophy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

{nonarteritic anterior ischemic optic neuropathy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {nonarteritic anterior ischemic optic neuropathy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 2, x-linked Gene Set

From OMIM Gene-Disease Associations

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

optic atrophy 3 with cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma of optic nerve Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma of optic nerve phenotype from the curated OMIM Gene-Disease Associations dataset.

polymicrogyria with optic nerve hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the polymicrogyria with optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

optic nerve hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

?neurodegeneration with optic atrophy, childhood onset Gene Set

From OMIM Gene-Disease Associations

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

optic atrophy plus syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

{leber optic atrophy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

optic cup Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

optic ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

optic nerve Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

optic lobe Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Diffuse mesangial sclerosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diffuse mesangial sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 1, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 1, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile primary lateral sclerosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile primary lateral sclerosis phenotype from the curated ClinVar Gene-Phenotype 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.

Amyotrophic lateral sclerosis 6, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 16, juvenile Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 16, juvenile phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteopathia striata with cranial sclerosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopathia striata with cranial sclerosis 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.

Amyotrophic Lateral Sclerosis 5 Gene Set

From CTD Gene-Disease Associations

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

Tuberous Sclerosis 2 Gene Set

From CTD Gene-Disease Associations

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

Tuberous Sclerosis 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tuberous Sclerosis 1 from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 6, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

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

Sclerosis Gene Set

From CTD Gene-Disease Associations

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

Osteopathia striata cranial sclerosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteopathia striata cranial sclerosis from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 11 Gene Set

From CTD Gene-Disease Associations

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

Amyotrophic Lateral Sclerosis, Sporadic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyotrophic Lateral Sclerosis, Sporadic from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 4, Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 4, Juvenile from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 3 from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 7 Gene Set

From CTD Gene-Disease Associations

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

Amyotrophic Lateral Sclerosis 8 Gene Set

From CTD Gene-Disease Associations

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

Amyotrophic Lateral Sclerosis 9 Gene Set

From CTD Gene-Disease Associations

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

Diffuse Cerebral Sclerosis of Schilder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diffuse Cerebral Sclerosis of Schilder from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 10 Gene Set

From CTD Gene-Disease Associations

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

AMYOTROPHIC LATERAL SCLEROSIS 12 Gene Set

From CTD Gene-Disease Associations

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

Mesangial sclerosis, diffuse Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mesangial sclerosis, diffuse from the curated CTD Gene-Disease Associations dataset.

Primary lateral sclerosis juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Primary lateral sclerosis juvenile from the curated CTD Gene-Disease Associations dataset.

Tuberous Sclerosis Gene Set

From CTD Gene-Disease Associations

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

Amyotrophic lateral sclerosis 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyotrophic lateral sclerosis 1 from the curated CTD Gene-Disease Associations dataset.

Primary Lateral Sclerosis, Adult, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Primary Lateral Sclerosis, Adult, 1 from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis Gene Set

From CTD Gene-Disease Associations

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

Polycystic kidneys, severe infantile with tuberous sclerosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic kidneys, severe infantile with tuberous sclerosis 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.

Amyotrophic Lateral Sclerosis 2, Juvenile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 2, Juvenile from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis Gene Set

From dbGAP Gene-Trait Associations

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

Sclerosis Gene Set

From dbGAP Gene-Trait Associations

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

tuberous sclerosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

amyotrophic lateral sclerosis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

amyotrophic lateral sclerosis Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

lateral sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tuberous sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

amyotrophic lateral sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pulmonary systemic sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hodgkin's lymphoma, nodular sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

amyotrophic lateral sclerosis type 8 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease amyotrophic lateral sclerosis type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

choroidal sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

amyotrophic lateral sclerosis Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; hemochromatosis Gene Set

From GAD Gene-Disease Associations

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

diffuse mesangial sclerosis Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; chromosome disorders; Gene Set

From GAD Gene-Disease Associations

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

sclerosis Gene Set

From GAD Gene-Disease Associations

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

seizures; thrombosis, deep vein; systemic sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease seizures; thrombosis, deep vein; systemic sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

syndrome mimicking amyotrophic lateral sclerosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease syndrome mimicking amyotrophic lateral sclerosis. 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.

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.

amyotrophic lateral sclerosis; Gene Set

From GAD Gene-Disease Associations

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

angiomyolipoma; dna damage; kidney neoplasms; tuberous sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angiomyolipoma; dna damage; kidney neoplasms; tuberous sclerosis 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.

epilepsy, temporal lobe; sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, temporal lobe; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diffuse systemic sclerosis Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis cause novel protein interactions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis cause novel protein interactions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tuberous sclerosis Gene Set

From GAD Gene-Disease Associations

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

systemic sclerosis Gene Set

From GAD Gene-Disease Associations

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

epilepsy, temporal lobe; sclerosis; seizures, febrile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, temporal lobe; sclerosis; seizures, febrile in GWAS and other genetic association datasets from the GAD 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.

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.

lupus erythematosus; sclerosis, systemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; sclerosis, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diffuse cerebral sclerosis of schilder; headache; seizures; [d]pain in head nos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial amyotrophic lateral sclerosis. Gene Set

From GAD Gene-Disease Associations

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

tuberous sclerosis phenotypes Gene Set

From GAD Gene-Disease Associations

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

cysts; epilepsy; tuberous sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cysts; epilepsy; tuberous sclerosis 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.

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.

familial amyotrophic lateral sclerosis Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; bone resorption; lead poisoning Gene Set

From GAD Gene-Disease Associations

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

confusion; epilepsy, temporal lobe; sclerosis; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease confusion; epilepsy, temporal lobe; sclerosis; seizures 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.

hypoxia ; systemic sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypoxia ; systemic sclerosis 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.

aortic valve sclerosis Gene Set

From GAD Gene-Disease Associations

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

sclerosis, systemic Gene Set

From GAD Gene-Disease Associations

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

hiv; sclerosis, systemic Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; craniocerebral trauma; injuries, craniocerebral Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; anoxia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; anoxia; 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.

als/amyotrophic lateral sclerosis Gene Set

From GAD Gene-Disease Associations

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

coronary stenosis; hypertrophy, left ventricular; sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary stenosis; hypertrophy, left ventricular; sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyotrophic lateral sclerosis; spastic paraplegia, hereditary Gene Set

From GAD Gene-Disease Associations

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

tuberous sclerosis 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tuberous sclerosis 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sclerosis Gene Set

From GeneRIF Biological Term Annotations

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

Amyotrophic lateral sclerosis (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Systemic lupus erythematosus and Systemic sclerosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systemic lupus erythematosus and Systemic sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hippocampal sclerosis of aging Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hippocampal sclerosis of aging phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Amyotrophic lateral sclerosis (sporadic) Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Systemic sclerosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Amyotrophic lateral sclerosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

amyotrophic lateral sclerosis Gene Set

From GWASdb SNP-Disease Associations

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

pulmonary systemic sclerosis Gene Set

From GWASdb SNP-Disease Associations

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

clavicular sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

cortical sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

sclerosis of skull base Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

diaphyseal sclerosis of the upper limbs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the diaphyseal sclerosis of the upper limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

diffuse mesangial sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

diaphyseal sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

amyotrophic lateral sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

metaphyseal sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

sclerosis of humeral diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

diffuse cerebral sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

sclerosis of finger phalanx Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of finger phalanx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

humeral sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

sclerosis of hand bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of hand bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

sclerosis of foot bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of foot bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

urethral sphincter sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

vertebral body sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

sclerosis of metaphyses of the upper limbs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the sclerosis of metaphyses of the upper limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

costochondral joint sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

choroidal sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

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

patchy sclerosis of radial diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the patchy sclerosis of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

amyotrophic lateral sclerosis Gene Set

From HPO Gene-Disease Associations

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

irregular sclerosis of hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular sclerosis of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse mesangial sclerosis Gene Set

From HPO Gene-Disease Associations

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

patchy sclerosis of finger phalanx Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy sclerosis of finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

metaphyseal sclerosis Gene Set

From HPO Gene-Disease Associations

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

patchy sclerosis of hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy sclerosis of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerosis of distal finger phalanx Gene Set

From HPO Gene-Disease Associations

genes associated with the sclerosis of distal finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

choroidal sclerosis Gene Set

From HPO Gene-Disease Associations

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

metatarsal diaphyseal endosteal sclerosis Gene Set

From HPO Gene-Disease Associations

genes associated with the metatarsal diaphyseal endosteal sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerosis of skull base Gene Set

From HPO Gene-Disease Associations

genes associated with the sclerosis of skull base 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.

vertebral body sclerosis Gene Set

From HPO Gene-Disease Associations

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

diffuse cerebral sclerosis Gene Set

From HPO Gene-Disease Associations

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

streaky metaphyseal sclerosis Gene Set

From HPO Gene-Disease Associations

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

clavicular sclerosis Gene Set

From HPO Gene-Disease Associations

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

diaphyseal cortical sclerosis Gene Set

From HPO Gene-Disease Associations

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

sclerosis of foot bone Gene Set

From HPO Gene-Disease Associations

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

metacarpal diaphyseal endosteal sclerosis Gene Set

From HPO Gene-Disease Associations

genes associated with the metacarpal diaphyseal endosteal sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerosis of hand bone Gene Set

From HPO Gene-Disease Associations

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

diaphyseal sclerosis Gene Set

From HPO Gene-Disease Associations

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

sclerosis of finger phalanx Gene Set

From HPO Gene-Disease Associations

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

Sclerosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tuberous Sclerosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Diffuse Cerebral Sclerosis of Schilder Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Amyotrophic Lateral Sclerosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 12 protein, mammalian Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 12 protein, mammalian protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 12 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 12 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

amyotrophic lateral sclerosis Gene Set

From KEGG Pathways

proteins participating in the amyotrophic lateral sclerosis pathway from the KEGG Pathways 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 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 2, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 2, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 16, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 16, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

primary lateral sclerosis, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the primary lateral sclerosis, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 3 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.

amyotrophic lateral sclerosis 4, juvenile Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 4, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.

?{amyotrophic lateral sclerosis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

amyotrophic lateral sclerosis 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

primary lateral sclerosis, adult, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the primary lateral sclerosis, adult, 1 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.

amyotrophic lateral sclerosis 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

polycystic kidney disease, infantile severe, with tuberous sclerosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the polycystic kidney disease, infantile severe, with tuberous sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopathia striata with cranial sclerosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopathia striata with cranial sclerosis 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 5, juvenile recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 5, juvenile recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

tuberous sclerosis-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tuberous sclerosis-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

tuberous sclerosis-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the tuberous sclerosis-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{amyotrophic lateral sclerosis, susceptibility to, 13} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {amyotrophic lateral sclerosis, susceptibility to, 13} phenotype from the curated OMIM Gene-Disease Associations dataset.

{amyotrophic lateral sclerosis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {amyotrophic lateral sclerosis, susceptibility to} 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 10, with or without ftd Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 10, with or without ftd phenotype from the curated OMIM Gene-Disease Associations dataset.

sclerosis Gene Set

From Phosphosite Textmining Biological Term Annotations

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

Amyotrophic lateral sclerosis (ALS)(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Amyotrophic lateral sclerosis (ALS)(Homo sapiens) pathway from the Wikipathways Pathways dataset.

tuberous sclerosis Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease tuberous sclerosis from the curated PhosphoSitePlus Phosphosite-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 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.

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.

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.

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 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 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.

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.

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 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.

MULTIPLE SYNOSTOSES SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE SYNOSTOSES SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Trichoepithelioma, Multiple Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 1 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 3 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 2 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 5 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 4 from the curated CTD Gene-Disease Associations dataset.

Multiple Myeloma Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Multiple Myeloma in GWAS and other genetic association datasets from the dbGAP Gene-Trait 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.

hereditary multiple exostoses Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

multiple epiphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

multiple carboxylase deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

multiple myeloma Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

multiple intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple myeloma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary multiple exostoses Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple mucosal neuroma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple chemical sensitivity Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple symmetrical lipomatosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple epiphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple carboxylase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple symmetric lipomatosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

multiple personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

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.

critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome 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.

melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; sepsis; shock, septic; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; sepsis; shock, septic; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; pancreatitis Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; sepsis; wounds and injuries Gene Set

From GAD Gene-Disease Associations

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

adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

multiple epiphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

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

burns; multiple organ failure; shock Gene Set

From GAD Gene-Disease Associations

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

leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma 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.

abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; respiratory distress syndrome, adult; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; respiratory distress syndrome, adult; sepsis 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.

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

From GAD Gene-Disease Associations

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

multiple myeloma; recurrence Gene Set

From GAD Gene-Disease Associations

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

hamartoma syndrome, multiple Gene Set

From GAD Gene-Disease Associations

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

multiple myeloma; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

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

multiple myeloma Gene Set

From GAD Gene-Disease Associations

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

leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

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

jaw diseases; multiple myeloma; osteonecrosis Gene Set

From GAD Gene-Disease Associations

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

adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple epiphyseal dysplasia; pseudoachondroplasia Gene Set

From GAD Gene-Disease Associations

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

head and neck neoplasms; neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head and neck neoplasms; neoplasms, multiple primary 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.

multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

multiple familial trichoepithelioma and familial cylindromatosis Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

lymphoma; multiple myeloma Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; sepsis; systemic infection; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; sepsis; systemic infection; wounds and injuries 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.

abnormalities, multiple; syndrome Gene Set

From GAD Gene-Disease Associations

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

multiple autoimmune diseases Gene Set

From GAD Gene-Disease Associations

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

multiple endocrine neoplasia type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection Gene Set

From GAD Gene-Disease Associations

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

carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

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

multiple myeloma; plasmacytoma Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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.

multiple chemical sensitivity Gene Set

From GAD Gene-Disease Associations

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

leukemia; multiple myeloma Gene Set

From GAD Gene-Disease Associations

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

pseudoachondroplasia and multiple epiphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, multiple primary; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; pneumonia; septic shock; shock, septic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; pneumonia; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; short bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; short bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms 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.

tic; combined vocal and multiple motor; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tic; combined vocal and multiple motor; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

multiple endocrine neoplasia type 2b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 2b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 2a Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 2a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leiomyoma; neoplasms, multiple primary; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leiomyoma; neoplasms, multiple primary; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; multiple myeloma; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

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

myeloma, multiple Gene Set

From GAD Gene-Disease Associations

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

carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

multiple oesophageal dysplasia Gene Set

From GAD Gene-Disease Associations

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

carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary multiple exostoses Gene Set

From GAD Gene-Disease Associations

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

breast neoplasms; neoplasms, multiple primary; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; neoplasms, multiple primary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; wounds and injuries Gene Set

From GAD Gene-Disease Associations

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

multiple myeloma; pneumonia; sepsis Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; multiple myeloma Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; sepsis Gene Set

From GAD Gene-Disease Associations

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

bone diseases; multiple myeloma Gene Set

From GAD Gene-Disease Associations

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

lymphoproliferative disorders; multiple myeloma Gene Set

From GAD Gene-Disease Associations

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

adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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.

abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia 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.

multiple myeloma; neoplasm recurrence, local Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; neoplasm recurrence, local 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 Gene Set

From GeneRIF Biological Term Annotations

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

Multiple benign melanocytic nevi_Epidermis_GSE3189 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Multiple benign melanocytic nevi_Epidermis_GSE3189 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Multiple myeloma Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Multiple myeloma (IgH translocation) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple myeloma (IgH translocation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple myeloma (hyperdiploidy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple myeloma (hyperdiploidy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

multiple myeloma Gene Set

From GWASdb SNP-Disease Associations

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

multiple mitochondrial dna deletions Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the multiple mitochondrial dna deletions phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

multiple myeloma Gene Set

From GWASdb SNP-Phenotype Associations

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

multiple exostoses Gene Set

From HPO Gene-Disease Associations

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

multiple epiphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

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

multiple gastric polyps Gene Set

From HPO Gene-Disease Associations

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

multiple cutaneous leiomyomas Gene Set

From HPO Gene-Disease Associations

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

multiple impacted teeth Gene Set

From HPO Gene-Disease Associations

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

multiple enchondromatosis Gene Set

From HPO Gene-Disease Associations

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

multiple prenatal fractures Gene Set

From HPO Gene-Disease Associations

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

multiple joint contractures Gene Set

From HPO Gene-Disease Associations

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

multiple rows of eyelashes Gene Set

From HPO Gene-Disease Associations

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

multiple myeloma Gene Set

From HPO Gene-Disease Associations

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

multiple plantar creases Gene Set

From HPO Gene-Disease Associations

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

multiple small vertebral fractures Gene Set

From HPO Gene-Disease Associations

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

ventricular preexcitation with multiple accessory pathways Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular preexcitation with multiple accessory pathways phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple digital exostoses Gene Set

From HPO Gene-Disease Associations

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

bowing of limbs due to multiple fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple glomerular cysts Gene Set

From HPO Gene-Disease Associations

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

multiple suture craniosynostosis Gene Set

From HPO Gene-Disease Associations

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

multiple lipomas Gene Set

From HPO Gene-Disease Associations

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

abnormality of multiple cell lineages in the bone marrow Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of multiple cell lineages in the bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple carpal ossification centers Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple carpal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple mitochondrial dna deletions Gene Set

From HPO Gene-Disease Associations

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

multiple pterygia Gene Set

From HPO Gene-Disease Associations

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

multiple small medullary renal cysts Gene Set

From HPO Gene-Disease Associations

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

multiple cafe-au-lait spots Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple cafe-au-lait spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple palmar creases Gene Set

From HPO Gene-Disease Associations

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

multiple rib fractures Gene Set

From HPO Gene-Disease Associations

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

multiple lentigines Gene Set

From HPO Gene-Disease Associations

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

multiple renal cysts Gene Set

From HPO Gene-Disease Associations

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

multiple skeletal anomalies Gene Set

From HPO Gene-Disease Associations

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

Multiple Trauma Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Multiple Organ Failure Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Multiple Endocrine Neoplasia Type 2b Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Endocrine Neoplasia Type 2b phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Endocrine Neoplasia Type 2a Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Endocrine Neoplasia Type 2a phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Myeloma Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Exostoses, Multiple Hereditary Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Abnormalities, Multiple Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hamartoma Syndrome, Multiple Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Multiple Endocrine Neoplasia Type 1 Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Endocrine Neoplasia Type 1 phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Acyl Coenzyme A Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Endocrine Neoplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Endocrine Neoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype 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 Chemical Sensitivity Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Neoplasms, Multiple Primary Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

multiple major aortopulmonary collateral arteries Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal atresia, multiple Gene Set

From OMIM Gene-Disease Associations

genes associated with the intestinal atresia, multiple phenotype from the curated OMIM Gene-Disease Associations dataset.

?epiphyseal dysplasia, multiple, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epiphyseal dysplasia, multiple, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 5, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 5, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

adenomas, multiple colorectal Gene Set

From OMIM Gene-Disease Associations

genes associated with the adenomas, multiple colorectal phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 9, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 9, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple endocrine neoplasia iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple endocrine neoplasia iib phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple endocrine neoplasia iia Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple endocrine neoplasia iia phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple pterygium syndrome, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 3, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 3, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple myeloma, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

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

cataract 1, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 1, multiple types phenotype from the curated OMIM Gene-Disease 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.

orolaryngeal cancer, multiple, Gene Set

From OMIM Gene-Disease Associations

genes associated with the orolaryngeal cancer, multiple, phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple fibroadenomas of the breast Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple fibroadenomas of the breast phenotype from the curated OMIM 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.

epiphyseal dysplasia, multiple, with myopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 20, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 20, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocephaly with multiple epiphyseal dysplasia and distinctive facies Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocephaly with multiple epiphyseal dysplasia and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple mitochondrial dysfunctions syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple mitochondrial dysfunctions syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple mitochondrial dysfunctions syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 14, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 14, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

venous malformations, multiple cutaneous and mucosal Gene Set

From OMIM Gene-Disease Associations

genes associated with the venous malformations, multiple cutaneous and mucosal phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 12, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 12, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 39, multiple types, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, with myopia and deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, with myopia and deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple endocrine neoplasia, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple endocrine neoplasia, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple endocrine neoplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple endocrine neoplasia 1 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.

cataract 34, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 34, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 11, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 11, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 6, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 6, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 2, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 2, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple myeloma, resistance to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple myeloma, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

genes associated with the pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 16, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 16, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 15, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 15, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple sulfatase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple sulfatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple synostoses syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple synostoses syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple synostoses syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple synostoses syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple synostoses syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple synostoses syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

exostoses, multiple, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the exostoses, multiple, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

exostoses, multiple, type 3 Gene Set

From OMIM Gene-Disease Associations

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

exostoses, multiple, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the exostoses, multiple, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 17, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 17, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 4, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 4, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 31, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 31, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 10, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 10, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple mitochondrial dysfunctions syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

trichoepithelioma, multiple familial, 1 Gene Set

From OMIM Gene-Disease Associations

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

trichoepithelioma, multiple familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichoepithelioma, multiple familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple self-healing squamous epithelioma, susceptiblity to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple self-healing squamous epithelioma, susceptiblity to} phenotype from the curated OMIM Gene-Disease Associations dataset.

Resolution of AP sites via the multiple-nucleotide patch replacement pathway Gene Set

From Reactome Pathways

proteins participating in the Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway from the Reactome Pathways dataset.

Defective HLCS causes multiple carboxylase deficiency Gene Set

From Reactome Pathways

proteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways dataset.

multiple myeloma cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

multiple myeloma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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