Name

Emery-dreifuss muscular dystrophy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy 7, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy 7, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Emery-Dreifuss muscular dystrophy 1, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Emery-Dreifuss muscular dystrophy 1, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular Dystrophy, Emery-Dreifuss Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Emery-Dreifuss from the curated CTD Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease emery-dreifuss muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

emery-dreifuss muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

Muscular Dystrophy, Emery-Dreifuss Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophy, Emery-Dreifuss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 2, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 3, ar Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 3, ar phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 6, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 6, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 1, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 1, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 5, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 5, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

emery-dreifuss muscular dystrophy 7, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the emery-dreifuss muscular dystrophy 7, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

Emery-Dreifuss muscular dystrophy Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Emery-Dreifuss muscular dystrophy from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

becker muscular dystrophy; duchenne muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

dreifuss Gene Set

From GeneRIF Biological Term Annotations

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

emery Gene Set

From GeneRIF Biological Term Annotations

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

muscular atrophy, spinal; spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

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

muscular dystrophies; muscular dystrophies, limb-girdle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophies; muscular dystrophies, limb-girdle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Duchenne muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Merosin deficient congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Walker-Warburg congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Limb-girdle muscular dystrophy, type 2S Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Becker muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eichsfeld type congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facioscapulohumeral muscular dystrophy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ullrich congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Miyoshi Muscular Dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miyoshi Muscular Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Miyoshi Muscular Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miyoshi Muscular Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.

Facioscapulohumeral muscular dystrophy 1a Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facioscapulohumeral muscular dystrophy 1a from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Animal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Animal from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2F from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy congenital, merosin negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.

Scleroatonic muscular dystrophy Gene Set

From CTD Gene-Disease Associations

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

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1 from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2C from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2J from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2L from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Facioscapulohumeral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Facioscapulohumeral from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Muscular Dystrophy, Oculopharyngeal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Oculopharyngeal from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 1B from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Merosin-Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2H from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy, type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy, type 2E from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 1C from the curated CTD Gene-Disease Associations dataset.

Facioscapulohumeral Muscular Dystrophy 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facioscapulohumeral Muscular Dystrophy 1B from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy, limb-girdle, type 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy, limb-girdle, type 1A from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Limb-Girdle, Type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Limb-Girdle, Type 2G from the curated CTD Gene-Disease Associations dataset.

Limb-girdle muscular dystrophy type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-girdle muscular dystrophy type 2A from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5 from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysa bullosa simplex and limb girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Muscular Dystrophy, Duchenne Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Duchenne from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Lmna-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.

Limb-Girdle Muscular Dystrophy, Type 1G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb-Girdle Muscular Dystrophy, Type 1G from the curated CTD Gene-Disease Associations dataset.

oculopharyngeal muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

limb-girdle muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease limb-girdle muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

facioscapulohumeral muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

ullrich congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

distal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

oculopharyngeal muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

facioscapulohumeral muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

limb-girdle muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ullrich congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

becker muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

duchenne muscular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular dystrophy-dystroglycanopathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set

From GAD Gene-Disease Associations

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

mental retardation; muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

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

muscular dystrophy, oculopharyngeal Gene Set

From GAD Gene-Disease Associations

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

ullrich congenital muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

duchenne muscular dystrophy Gene Set

From GAD Gene-Disease Associations

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

muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

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

Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1472 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE1026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Extraocular muscle_GSE1008 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Duchenne muscular dystrophy (DMD)_Muscle - Striated (Skeletal) (MMHCC)_GSE1025 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

limb-girdle muscular dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the limb-girdle muscular dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular dystrophy Gene Set

From HPO Gene-Disease Associations

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

congenital muscular dystrophy Gene Set

From HPO Gene-Disease Associations

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

Muscular Dystrophy, Facioscapulohumeral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Dystrophy, Duchenne Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

fascioscapulohumeral muscular dystrophy 2, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the fascioscapulohumeral muscular dystrophy 2, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, megaconial type Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, megaconial type phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to partial lama2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, due to itga7 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, due to itga7 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?muscular dystrophy, limb-girdle, type 2r Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?muscular dystrophy, limb-girdle, type 2r phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, rigid spine, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, rigid spine, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, merosin-positive Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, merosin-positive phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2q Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2q phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2s Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2s phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2e Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2f Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2f phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2g Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2g phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2l Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2l phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2h Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2h phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 2j Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 2j phenotype from the curated OMIM Gene-Disease Associations dataset.

ullrich congenital muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ullrich congenital muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

tibial muscular dystrophy, tardive Gene Set

From OMIM Gene-Disease Associations

genes associated with the tibial muscular dystrophy, tardive phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1h Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1h phenotype from the curated OMIM Gene-Disease Associations dataset.

oculopharyngeal muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculopharyngeal muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

miyoshi muscular dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the miyoshi muscular dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

duchenne muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the duchenne muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (limb-girdle), type c, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

limb-girdle muscular dystrophy, type 1g Gene Set

From OMIM Gene-Disease Associations

genes associated with the limb-girdle muscular dystrophy, type 1g phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy with rimmed vacuoles Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy with rimmed vacuoles phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

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

From OMIM Gene-Disease Associations

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

muscular dystrophy with epidermolysis bullosa simplex Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy with epidermolysis bullosa simplex phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

becker muscular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the becker muscular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital, 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

muscular dystrophy, limb-girdle, type ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1e Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1e phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1f Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1f phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, limb-girdle, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, limb-girdle, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy, congenital merosin-deficient Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy, congenital merosin-deficient phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

cone-rod dystrophy 6, 60177 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 6, 60177 phenotype from the curated OMIM Gene-Disease Associations dataset.

Spinal muscular atrophy, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, X-linked 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular hypertrophy-cerebral syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, autosomal recessive 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinal muscular atrophy, Jerash type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophies, Limb-Girdle Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophies, Limb-Girdle from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

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

Spinal muscular atrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.

Spinal muscular atrophy with respiratory distress 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.

Muscular Atrophy Gene Set

From CTD Gene-Disease Associations

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

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophies Gene Set

From CTD Gene-Disease Associations

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

Muscular Diseases Gene Set

From CTD Gene-Disease Associations

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

Spinal Muscular Atrophies of Childhood Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.

SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.

Muscular Atrophy, Spinal Gene Set

From CTD Gene-Disease Associations

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

Muscular Diseases Gene Set

From dbGAP Gene-Trait Associations

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

spinal muscular atrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

atrophic muscular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

muscular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

muscular disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

atrophic muscular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

adult spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

juvenile spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

intermediate spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

progressive muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

survival motor neuron spinal muscular atrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

muscular atrophy; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophies, limb-girdle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophies, limb-girdle 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.

disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; muscular diseases Gene Set

From GAD Gene-Disease Associations

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

lipid metabolism disorders; muscular diseases Gene Set

From GAD Gene-Disease Associations

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

graves disease; muscular diseases Gene Set

From GAD Gene-Disease Associations

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

spinal muscular atrophies of childhood Gene Set

From GAD Gene-Disease Associations

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

muscular diseases Gene Set

From GAD Gene-Disease Associations

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

muscular atrophy, spinal Gene Set

From GAD Gene-Disease Associations

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

cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, dilated; cardiomyopathy, hypertrophic; muscular dystrophies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal muscular atrophy Gene Set

From GAD Gene-Disease Associations

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

muscular dystrophies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease muscular dystrophies 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.

spinal muscular atrophy phenotype Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; diabetes mellitus; muscular diseases; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases; muscular dystrophies Gene Set

From GAD Gene-Disease Associations

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

muscular disorders, atrophic Gene Set

From GAD Gene-Disease Associations

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

disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; hypercholesterolemia; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; hypercholesterolemia; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular Gene Set

From GeneRIF Biological Term Annotations

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

Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2629 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) - Diaphragm (MMHCC)_GSE3252 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Neurogenic Muscular Atrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2566 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Muscular Dystrophy_Muscle - Striated (Skeletal) (MMHCC)_GSE2507 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

muscular septum morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the muscular septum morphogenesis biological process from the curated GO Biological Process Annotations dataset.

muscular atrophy Gene Set

From GWASdb SNP-Disease Associations

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

muscular disease Gene Set

From GWASdb SNP-Disease Associations

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

muscular hypotonia Gene Set

From GWASdb SNP-Phenotype Associations

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

congenital muscular torticollis Gene Set

From HPO Gene-Disease Associations

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

extrapyramidal muscular rigidity Gene Set

From HPO Gene-Disease Associations

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

muscular edema Gene Set

From HPO Gene-Disease Associations

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

muscular hypotonia Gene Set

From HPO Gene-Disease Associations

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

progressive distal muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

infantile muscular hypotonia Gene Set

From HPO Gene-Disease Associations

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

nonprogressive muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

muscular hypotonia of the trunk Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular hypotonia of the trunk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal muscular atrophy Gene Set

From HPO Gene-Disease Associations

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

severe muscular hypotonia Gene Set

From HPO Gene-Disease Associations

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

generalized muscular appearance from birth Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized muscular appearance from birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Muscular Dystrophies, Limb-Girdle Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Muscular Dystrophies, Limb-Girdle phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Muscular Disorders, Atrophic Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Dystrophies Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spinal Muscular Atrophies of Childhood Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Atrophy, Spinal Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Muscular LMNA-interacting protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Muscular LMNA-interacting protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Small muscular protein Chisel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Small muscular protein Chisel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal interventricular septum muscular part morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal interventricular septum muscular part morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

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

spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy with progressive myoclonic epilepsy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, x-linked 2, infantile Gene Set

From OMIM Gene-Disease Associations

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

spinal muscular atrophy-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy-3 Gene Set

From OMIM Gene-Disease Associations

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

spinal muscular atrophy-1 Gene Set

From OMIM Gene-Disease Associations

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

spinal muscular atrophy-4 Gene Set

From OMIM Gene-Disease Associations

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

spinal muscular atrophy, chronic distal, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, jokela type Gene Set

From OMIM Gene-Disease Associations

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

scapuloperoneal spinal muscular atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

{spinal muscular atrophy, type iii, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, x-linked 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal and bulbar muscular atrophy of kennedy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, congenital nonprogressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue muscular system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

vertebrate muscular system Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue vertebrate muscular system from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

muscular system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue muscular system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

vertebrate muscular system Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue vertebrate muscular system in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

muscular coat Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

invertebrate muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

vertebrate muscular system Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Patterned dystrophy of retinal pigment epithelium Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular dystrophy, vitelliform, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular dystrophy, vitelliform, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MACULAR CORNEAL DYSTROPHY, TYPE II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MACULAR CORNEAL DYSTROPHY, TYPE II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asphyxiating thoracic dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asphyxiating thoracic dystrophy 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Asphyxiating thoracic dystrophy 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Asphyxiating thoracic dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fleck corneal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fleck corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Occult macular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Occult macular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular corneal dystrophy Type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy and perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bietti crystalline corneoretinal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bietti crystalline corneoretinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy Type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy Type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone dystrophy 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone dystrophy 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thiel-Behnke corneal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thiel-Behnke corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Reis-Bucklers' corneal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Reis-Bucklers' corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy, X-linked 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vitelliform dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitelliform dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy, fuchs endothelial, 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy, fuchs endothelial, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy, fuchs endothelial, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy, fuchs endothelial, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy, fuchs endothelial, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy, fuchs endothelial, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy Fuchs endothelial 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy Fuchs endothelial 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schnyder crystalline corneal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schnyder crystalline corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal cone dystrophy 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONE DYSTROPHY 5, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONE DYSTROPHY 5, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy type 3A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy type 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile neuroaxonal dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile neuroaxonal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macular dystrophy, vitelliform, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macular dystrophy, vitelliform, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal endothelial dystrophy type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal endothelial dystrophy type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal cone dystrophy 3B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal cone dystrophy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, early-onset severe Gene Set

From ClinVar Gene-Phenotype Associations

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

Cone-rod dystrophy amelogenesis imperfecta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy amelogenesis imperfecta phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lattice corneal dystrophy Type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lattice corneal dystrophy Type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cone-rod dystrophy 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cone-rod dystrophy 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Groenouw corneal dystrophy type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Groenouw corneal dystrophy type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal epithelial dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal epithelial dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Stromal Corneal Dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy, gelatinous drop-like Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, gelatinous drop-like from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Juvenile Epithelial of Meesmann Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Juvenile Epithelial of Meesmann from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 3A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 3A from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, retinal, 1, North Carolina type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, retinal, 1, North Carolina type from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 8 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 7 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 5 Gene Set

From CTD Gene-Disease Associations

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

Corneal dystrophy Avellino type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy Avellino type from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 3B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 3B from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 6 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 3 from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, atypical vitelliform Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, atypical vitelliform from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, concentric annular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, concentric annular from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 13 Gene Set

From CTD Gene-Disease Associations

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

Corneal Dystrophy, Endothelial, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Endothelial, X-Linked from the curated CTD Gene-Disease Associations dataset.

Macular Dystrophy, Retinal, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular Dystrophy, Retinal, 2 from the curated CTD Gene-Disease Associations dataset.

Lattice corneal dystrophy type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lattice corneal dystrophy type 1 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, Fuchs' endothelial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 2 from the curated CTD Gene-Disease Associations dataset.

Bullous Dystrophy, Hereditary Macular Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bullous Dystrophy, Hereditary Macular Type from the curated CTD Gene-Disease Associations dataset.

Reflex Sympathetic Dystrophy Gene Set

From CTD Gene-Disease Associations

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

Corneal Dystrophy, Crystalline, of Schnyder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Crystalline, of Schnyder from the curated CTD Gene-Disease Associations dataset.

Cone Dystrophy 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone Dystrophy 3 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, Fuchs' endothelial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, Fuchs' endothelial, 1 from the curated CTD Gene-Disease Associations dataset.

Patterned dystrophy of retinal pigment epithelium Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Patterned dystrophy of retinal pigment epithelium from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Lisch Epithelial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Lisch Epithelial from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, epithelial basement membrane Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, epithelial basement membrane from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy and perceptive deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy and perceptive deafness from the curated CTD Gene-Disease Associations dataset.

MACULAR DYSTROPHY, RETINAL, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MACULAR DYSTROPHY, RETINAL, 3 from the curated CTD Gene-Disease Associations dataset.

Bothnia Retinal Dystrophy Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy, X-Linked, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy, X-Linked, 2 from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy, X-Linked, 3 Gene Set

From CTD Gene-Disease Associations

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

Cone Dystrophy 4 Gene Set

From CTD Gene-Disease Associations

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

Corneal endothelial dystrophy type 2 Gene Set

From CTD Gene-Disease Associations

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

CONE-ROD DYSTROPHY 9 Gene Set

From CTD Gene-Disease Associations

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

CONE-ROD DYSTROPHY 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONE-ROD DYSTROPHY 2 from the curated CTD Gene-Disease Associations dataset.

Doyne honeycomb retinal dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Doyne honeycomb retinal dystrophy from the curated CTD Gene-Disease Associations dataset.

Bietti Crystalline Dystrophy Gene Set

From CTD Gene-Disease Associations

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

OCCULT MACULAR DYSTROPHY Gene Set

From CTD Gene-Disease Associations

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

Choroidal Dystrophy, Central Areolar 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Choroidal Dystrophy, Central Areolar 2 from the curated CTD Gene-Disease Associations dataset.

Asphyxiating Thoracic Dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asphyxiating Thoracic Dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fleck Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fleck from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cone-Rod Dystrophy 1 from the curated CTD Gene-Disease Associations dataset.

Toenail Dystrophy, Isolated Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toenail Dystrophy, Isolated from the curated CTD Gene-Disease Associations dataset.

Retinal cone dystrophy 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal cone dystrophy 2 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Posterior Polymorphous, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 2 from the curated CTD Gene-Disease Associations dataset.

Fundus Dystrophy, Pseudoinflammatory, Of Sorsby Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fundus Dystrophy, Pseudoinflammatory, Of Sorsby from the curated CTD Gene-Disease Associations dataset.

Myotonic Dystrophy Gene Set

From CTD Gene-Disease Associations

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

Corneal Dystrophy, Fuchs Endothelial, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 7 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Posterior Polymorphous, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 1 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Posterior Polymorphous, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 3 from the curated CTD Gene-Disease Associations dataset.

CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT Gene Set

From CTD Gene-Disease Associations

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

Vitelliform Macular Dystrophy Gene Set

From CTD Gene-Disease Associations

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

Corneal Dystrophy, Congenital Stromal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset.

Choroidal dystrophy central areolar Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Choroidal dystrophy central areolar from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy, Thiel-Behnke type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy, Thiel-Behnke type from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy from the curated CTD Gene-Disease Associations dataset.

Cone-Rod Dystrophy 12 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 11 Gene Set

From CTD Gene-Disease Associations

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

Cone-Rod Dystrophy 10 Gene Set

From CTD Gene-Disease Associations

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

CONE-ROD DYSTROPHY, X-LINKED, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONE-ROD DYSTROPHY, X-LINKED, 1 from the curated CTD Gene-Disease Associations dataset.

Newfoundland Rod-Cone Dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Newfoundland Rod-Cone Dystrophy from the curated CTD Gene-Disease Associations dataset.

Groenouw type I corneal dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Groenouw type I corneal dystrophy from the curated CTD Gene-Disease Associations dataset.

CONE-ROD DYSTROPHY 15 Gene Set

From CTD Gene-Disease Associations

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

Corneal Dystrophy, Lattice Type IIIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Lattice Type IIIA from the curated CTD Gene-Disease Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.

Retinal Cone Dystrophy 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Cone Dystrophy 4 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 5 from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Fuchs Endothelial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Fuchs Endothelial, 4 from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy of Bowman layer, type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy of Bowman layer, type 1 from the curated CTD Gene-Disease Associations dataset.

Macular dystrophy, corneal type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macular dystrophy, corneal type 1 from the curated CTD Gene-Disease Associations dataset.

Fuchs Endothelial Dystrophy Gene Set

From dbGAP Gene-Trait Associations

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

cone-rod dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

asphyxiating thoracic dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

vitelliform macular dystrophy Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

myotonic dystrophy type 1 Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease myotonic dystrophy type 1 from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

partial central choroid dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

lattice corneal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vitelliform macular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal granular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary retinal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

corneal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

reflex sympathetic dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vulvar dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

occult macular dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fuchs' endothelial dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cone-rod dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

macular corneal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

asphyxiating thoracic dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bietti crystalline corneoretinal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

neuroaxonal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

fundus dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

vitreoretinal dystrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

myotonic dystrophy type 1 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease myotonic dystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

myotonic dystrophy type 2 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease myotonic dystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cone dystrophy Gene Set

From GAD Gene-Disease Associations

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

cone-rod dystrophy Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

granular corneal dystrophy Gene Set

From GAD Gene-Disease Associations

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

fuchs endothelial dystrophy Gene Set

From GAD Gene-Disease Associations

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

gelatinous droplike corneal dystrophy Gene Set

From GAD Gene-Disease Associations

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

myotonic dystrophy type 1 Gene Set

From GAD Gene-Disease Associations

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

macular corneal dystrophy. Gene Set

From GAD Gene-Disease Associations

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

corneal dystrophies, hereditary; hereditary corneal dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinitis pigmentosa; macular dystrophy Gene Set

From GAD Gene-Disease Associations

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

atrioventricular block; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

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

chromosome disorders; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

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

carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fuchs' endothelial dystrophy Gene Set

From GAD Gene-Disease Associations

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

lattice corneal dystrophy type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lattice corneal dystrophy type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cone-rod dystrophy; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cone-rod dystrophy; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibromyalgia; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

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

recessive cone-rod dystrophy Gene Set

From GAD Gene-Disease Associations

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

corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

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

macular corneal dystrophy Gene Set

From GAD Gene-Disease Associations

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

pain, postoperative; radius fractures; reflex sympathetic dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pain, postoperative; radius fractures; reflex sympathetic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystrophy Gene Set

From GeneRIF Biological Term Annotations

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

Fuchs's corneal dystrophy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fuchs's corneal dystrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

corneal dystrophy Gene Set

From GWASdb SNP-Disease Associations

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

nail dystrophy Gene Set

From HPO Gene-Disease Associations

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

polymorphous posterior corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the polymorphous posterior corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lattice corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

cone-rod dystrophy Gene Set

From HPO Gene-Disease Associations

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

macroreticular retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

congenital corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

granular corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

map-dot-fingerprint corneal dystrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the map-dot-fingerprint corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

speckled corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

crystalline corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

choroidal dystrophy Gene Set

From HPO Gene-Disease Associations

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

chorioretinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

marginal corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

nodular corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

nonprogressive congenital retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

juvenile epithelial corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

macular dystrophy Gene Set

From HPO Gene-Disease Associations

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

mosaic corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

punctate corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

reticular retinal dystrophy Gene Set

From HPO Gene-Disease Associations

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

corneal dystrophy Gene Set

From HPO Gene-Disease Associations

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

Reflex Sympathetic Dystrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Vitelliform Macular Dystrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Myotonic Dystrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Myotonic dystrophy protein kinase, coiled coil Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myotonic dystrophy protein kinase, coiled coil protein domain from the InterPro Predicted Protein Domain Annotations dataset.

nail dystrophy Gene Set

From MPO Gene-Phenotype Associations

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

axonal dystrophy Gene Set

From MPO Gene-Phenotype Associations

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

corneal dystrophy, schnyder type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, schnyder type phenotype from the curated OMIM Gene-Disease Associations dataset.

newfoundland rod-cone dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the newfoundland rod-cone dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy-3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bothnia retinal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the bothnia retinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

t-cell immunodeficiency, congenital alopecia, and nail dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the t-cell immunodeficiency, congenital alopecia, and nail dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

occult macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the occult macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal dystrophy, early-onset severe Gene Set

From OMIM Gene-Disease Associations

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

microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract with late-onset corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

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

corneal dystrophy, congenital stromal Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, congenital stromal phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, lattice type iiia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lattice type iiia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia, ectrodactyly, and macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

cone-rod dystrophy, x-linked, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy, x-linked, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, gelatinous drop-like Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, gelatinous drop-like phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod retinal dystrophy-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod retinal dystrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod retinal dystrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod retinal dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, retinal, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, retinal, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, retinal, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, retinal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, posterior polymorphous, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, posterior polymorphous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, posterior polymorphous, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, posterior polymorphous, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, fuchs endothelial, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, fuchs endothelial, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

toenail dystrophy, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the toenail dystrophy, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, epithelial basement membrane Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, epithelial basement membrane phenotype from the curated OMIM Gene-Disease Associations dataset.

hypotrichosis, congenital, with juvenile macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypotrichosis, congenital, with juvenile macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal endothelial dystrophy and perceptive deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal endothelial dystrophy and perceptive deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, north carolina type Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, north carolina type phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

retinol dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinol dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal endothelial dystrophy 1, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal endothelial dystrophy 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, reis-bucklers type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, reis-bucklers type phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, patterned, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, patterned, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, thiel-behnke type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, thiel-behnke type phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy with central cone involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy with central cone involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

cone dystrophy, progressive x-linked, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

choriodal dystrophy, central areolar 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the choriodal dystrophy, central areolar 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

myotonic dystrophy 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myotonic dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

myotonic dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myotonic dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, endothelial, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, endothelial, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

cone-rod dystrophy 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cone-rod dystrophy 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

infantile neuroaxonal dystrophy 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the infantile neuroaxonal dystrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal endothelial dystrophy 2, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal endothelial dystrophy 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

sorsby fundus dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the sorsby fundus dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

bietti crystalline corneoretinal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the bietti crystalline corneoretinal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

corneal dystrophy, lattice type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lattice type i phenotype from the curated OMIM Gene-Disease Associations dataset.

vitelliform macular dystrophy 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the vitelliform macular dystrophy 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, posterior polymorphous 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, posterior polymorphous 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, groenouw type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, groenouw type i phenotype from the curated OMIM Gene-Disease Associations dataset.

meesmann corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

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

corneal fleck dystrophy Gene Set

From OMIM Gene-Disease Associations

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

macular corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

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

?cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal cone dystrophy-1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal cone dystrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal cone dystrophy 3b Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, avellino type Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, avellino type phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal dystrophy, lisch epithelial Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal dystrophy, lisch epithelial phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, vitelliform, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, vitelliform, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, vitelliform, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, vitelliform, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

macular dystrophy, vitelliform, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the macular dystrophy, vitelliform, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

myotonic dystrophy type1 Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease myotonic dystrophy type1 from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

DG(22:6n3/0:0/22:6n3) Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the DG(22:6n3/0:0/22:6n3) metabolite from the curated HMDB Metabolites of Enzymes dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-6407-02B-11R-A36H-07,TCGA-DU-6407-02A-12R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-6407-02B-11R-A36H-07,TCGA-DU-6407-02A-12R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Brain Lower Grade Glioma_LGG_TCGA-DU-6404-02A-21R-A36H-07,TCGA-DU-6404-02B-11R-A36H-07 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Brain Lower Grade Glioma_LGG_TCGA-DU-6404-02A-21R-A36H-07,TCGA-DU-6404-02B-11R-A36H-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

697 Gene Set

From Achilles Cell Line Gene Essentiality Profiles

gene knockdowns changing fitness of 697 relative to other cell lines from the Achilles Cell Line Gene Essentiality Profiles dataset.

697 Gene Set

From CCLE Cell Line Gene CNV Profiles

genes with high or low copy number in 697 relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.

647V Gene Set

From CCLE Cell Line Gene CNV Profiles

genes with high or low copy number in 647V relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.

639V Gene Set

From CCLE Cell Line Gene CNV Profiles

genes with high or low copy number in 639V relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.

697 Gene Set

From CCLE Cell Line Gene Expression Profiles

genes with high or low expression in 697 relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.

647V Gene Set

From CCLE Cell Line Gene Expression Profiles

genes with high or low expression in 647V relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.

639V Gene Set

From CCLE Cell Line Gene Expression Profiles

genes with high or low expression in 639V relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.

697 Gene Set

From CCLE Cell Line Gene Mutation Profiles

genes mutated in the 697 cell line from the CCLE Cell Line Gene Mutation Profiles dataset.

647V Gene Set

From CCLE Cell Line Gene Mutation Profiles

genes mutated in the 647V cell line from the CCLE Cell Line Gene Mutation Profiles dataset.

639V Gene Set

From CCLE Cell Line Gene Mutation Profiles

genes mutated in the 639V cell line from the CCLE Cell Line Gene Mutation Profiles dataset.

ribavirin-6521 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ribavirin-6521 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

(+)-chelidonine-6236 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the (+)-chelidonine-6236 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PHA-00767505E-6596 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PHA-00767505E-6596 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PHA-00767505E-6591 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PHA-00767505E-6591 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

16,16-dimethylprostaglandin E2-6597 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 16,16-dimethylprostaglandin E2-6597 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

16,16-dimethylprostaglandin E2-6592 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 16,16-dimethylprostaglandin E2-6592 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PF-00562151-00-6907 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PF-00562151-00-6907 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

promazine-6028 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the promazine-6028 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tamoxifen-6768 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tamoxifen-6768 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

mercaptopurine-667 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the mercaptopurine-667 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dexibuprofen-6471 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dexibuprofen-6471 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-665-6041 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-665-6041 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bephenium hydroxynaphthoate-6466 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bephenium hydroxynaphthoate-6466 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

mephenytoin-6158 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the mephenytoin-6158 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

paclitaxel-6720 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the paclitaxel-6720 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

adrenosterone-6486 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the adrenosterone-6486 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

LY-294002-6186 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the LY-294002-6186 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cinoxacin-6257 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cinoxacin-6257 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

lorglumide-6456 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the lorglumide-6456 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-664-4275 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-664-4275 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cefmetazole-6086 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cefmetazole-6086 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

desoxycortone-6476 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the desoxycortone-6476 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

alpha-estradiol-6169 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the alpha-estradiol-6169 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

LY-294002-6987 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the LY-294002-6987 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

naftidrofuryl-6687 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the naftidrofuryl-6687 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-674-4738 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-674-4738 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nifenazone-6016 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nifenazone-6016 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-6579 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-6579 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

estradiol-6957 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the estradiol-6957 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

5707885-6390 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 5707885-6390 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfanilamide-6810 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfanilamide-6810 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

benserazide-6722 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the benserazide-6722 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

anabasine-6074 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the anabasine-6074 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cyproterone-6806 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cyproterone-6806 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

prazosin-6315 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the prazosin-6315 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ioversol-6726 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ioversol-6726 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

brinzolamide-6670 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the brinzolamide-6670 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tolfenamic acid-6354 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tolfenamic acid-6354 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

SR-95639A-6632 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the SR-95639A-6632 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bupropion-6256 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bupropion-6256 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dihydroergotamine-6840 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dihydroergotamine-6840 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

wortmannin-6959 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the wortmannin-6959 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

docosahexaenoic acid ethyl ester-664 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the docosahexaenoic acid ethyl ester-664 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxyphenbutazone-6844 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxyphenbutazone-6844 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-682-6638 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-682-6638 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

paclitaxel-640 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the paclitaxel-640 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

thiethylperazine-6154 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the thiethylperazine-6154 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-682-4984 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-682-4984 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

idazoxan-6747 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the idazoxan-6747 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

STOCK1N-35215-6380 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the STOCK1N-35215-6380 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

acemetacin-6361 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the acemetacin-6361 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

altizide-6829 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the altizide-6829 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methotrexate-6654 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methotrexate-6654 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

butyl hydroxybenzoate-6446 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the butyl hydroxybenzoate-6446 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

metergoline-6744 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the metergoline-6744 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

SB-202190-6909 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the SB-202190-6909 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

natamycin-6126 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the natamycin-6126 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

acacetin-6044 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the acacetin-6044 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clomipramine-6825 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clomipramine-6825 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

riboflavin-6822 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the riboflavin-6822 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

terguride-6299 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the terguride-6299 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-691-2813 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-691-2813 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chlorpromazine-6977 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chlorpromazine-6977 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-6671 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-6671 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfasalazine-6346 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfasalazine-6346 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ganciclovir-6289 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ganciclovir-6289 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

gallamine triethiodide-6215 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the gallamine triethiodide-6215 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

estriol-6140 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the estriol-6140 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ticarcillin-6146 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ticarcillin-6146 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dioxybenzone-6478 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dioxybenzone-6478 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-689-6076 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-689-6076 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

SC-560-6865 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the SC-560-6865 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-857-6635 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-857-6635 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fluspirilene-6662 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fluspirilene-6662 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

valproic acid-6181 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the valproic acid-6181 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

mesalazine-6162 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the mesalazine-6162 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

strophanthidin-6087 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the strophanthidin-6087 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ursodeoxycholic acid-6484 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ursodeoxycholic acid-6484 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

maprotiline-6676 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the maprotiline-6676 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tracazolate-6619 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tracazolate-6619 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

isopropamide iodide-6781 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the isopropamide iodide-6781 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

prochlorperazine-6664 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the prochlorperazine-6664 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

diltiazem-6710 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the diltiazem-6710 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dexibuprofen-6712 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dexibuprofen-6712 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nomegestrol-6362 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nomegestrol-6362 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

alpha-yohimbine-6274 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the alpha-yohimbine-6274 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

rolipram-6449 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the rolipram-6449 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

propofol-6707 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the propofol-6707 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

LM-1685-612 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the LM-1685-612 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

gossypol-6058 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the gossypol-6058 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

helveticoside-6047 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the helveticoside-6047 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

SB-203580-6894 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the SB-203580-6894 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

SB-203580-6899 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the SB-203580-6899 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylprednisolone-6785 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylprednisolone-6785 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

esculetin-6499 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the esculetin-6499 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ciclosporin-602 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ciclosporin-602 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ramifenazone-6097 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ramifenazone-6097 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

midecamycin-6745 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the midecamycin-6745 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methylergometrine-6704 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methylergometrine-6704 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chlorprothixene-6692 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chlorprothixene-6692 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

3-nitropropionic acid-6367 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 3-nitropropionic acid-6367 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nabumetone-6327 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nabumetone-6327 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

saquinavir-6127 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the saquinavir-6127 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clozapine-6188 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clozapine-6188 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

monastrol-681 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the monastrol-681 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

hydrochlorothiazide-6625 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the hydrochlorothiazide-6625 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

geldanamycin-6187 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the geldanamycin-6187 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfamerazine-6036 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfamerazine-6036 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

proxyphylline-6494 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the proxyphylline-6494 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

promethazine-6477 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the promethazine-6477 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sirolimus-6180 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sirolimus-6180 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-675-3682 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-675-3682 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cytisine-6217 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cytisine-6217 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nipecotic acid-6500 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nipecotic acid-6500 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-6085 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-6085 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

alfadolone-6506 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the alfadolone-6506 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-6736 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-6736 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

diclofenamide-6686 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the diclofenamide-6686 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

U0125-663 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the U0125-663 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trichostatin A-6551 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trichostatin A-6551 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

pilocarpine-6741 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the pilocarpine-6741 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chrysin-6485 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chrysin-6485 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

aconitine-6797 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the aconitine-6797 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dl-alpha tocopherol-6616 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dl-alpha tocopherol-6616 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-685-3683 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-685-3683 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

raloxifene-6235 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the raloxifene-6235 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fluorometholone-6071 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fluorometholone-6071 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chlorpromazine-6936 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chlorpromazine-6936 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-690334-01-3823 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-690334-01-3823 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-690334-01-3826 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-690334-01-3826 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

hydrocortisone-6684 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the hydrocortisone-6684 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fluvastatin-6691 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fluvastatin-6691 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

isometheptene-6524 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the isometheptene-6524 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chloropyrazine-6227 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chloropyrazine-6227 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nifurtimox-6608 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nifurtimox-6608 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

SB-202190-6882 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the SB-202190-6882 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

chlortetracycline-6761 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the chlortetracycline-6761 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

SB-202190-6887 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the SB-202190-6887 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

meropenem-6141 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the meropenem-6141 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methotrexate-6318 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methotrexate-6318 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

carbinoxamine-6786 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the carbinoxamine-6786 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dinoprostone-6552 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dinoprostone-6552 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

deptropine-6523 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the deptropine-6523 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

khellin-6641 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the khellin-6641 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

alvespimycin-6172 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the alvespimycin-6172 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tubocurarine chloride-6351 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tubocurarine chloride-6351 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

famotidine-6665 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the famotidine-6665 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

paracetamol-6284 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the paracetamol-6284 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

etynodiol-6479 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the etynodiol-6479 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

hydrocotarnine-6827 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the hydrocotarnine-6827 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clebopride-6311 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clebopride-6311 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

finasteride-6062 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the finasteride-6062 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

piperacetazine-6152 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the piperacetazine-6152 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

methanthelinium bromide-6254 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the methanthelinium bromide-6254 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

pyrazinamide-6617 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the pyrazinamide-6617 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-685-2188 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-685-2188 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fulvestrant-6997 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fulvestrant-6997 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

piribedil-6333 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the piribedil-6333 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

F0447-0125-6401 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the F0447-0125-6401 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

butirosin-666 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the butirosin-666 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-665-3681 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-665-3681 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

fulvestrant-6197 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the fulvestrant-6197 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nitrendipine-6464 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nitrendipine-6464 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nicardipine-6297 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nicardipine-6297 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

STOCK1N-35874-6561 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the STOCK1N-35874-6561 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxybutynin-6770 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxybutynin-6770 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-642-4594 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-642-4594 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

prasterone-6673 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the prasterone-6673 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

5155877-6574 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 5155877-6574 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PF-01378883-00-6405 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PF-01378883-00-6405 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

alprenolol-6789 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the alprenolol-6789 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

orlistat-6420 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the orlistat-6420 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

(-)-MK-801-6458 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the (-)-MK-801-6458 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

rosiglitazone-6992 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the rosiglitazone-6992 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

2-aminobenzenesulfonamide-6321 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 2-aminobenzenesulfonamide-6321 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

rosiglitazone-6192 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the rosiglitazone-6192 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nordihydroguaiaretic acid-6983 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nordihydroguaiaretic acid-6983 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PF-00562151-00-6868 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PF-00562151-00-6868 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PF-00562151-00-6863 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PF-00562151-00-6863 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

acepromazine-6832 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the acepromazine-6832 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clorgiline-6659 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clorgiline-6659 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

amitriptyline-6353 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the amitriptyline-6353 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

luteolin-6658 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the luteolin-6658 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tranexamic acid-6238 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tranexamic acid-6238 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

valproic acid-6974 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the valproic acid-6974 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

terbutaline-6240 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the terbutaline-6240 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

metyrapone-6447 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the metyrapone-6447 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

pipemidic acid-6752 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the pipemidic acid-6752 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-690334-01-4558 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-690334-01-4558 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

STOCK1N-28457-6906 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the STOCK1N-28457-6906 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

phenazopyridine-6100 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the phenazopyridine-6100 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cyclopentolate-6132 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cyclopentolate-6132 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

erythromycin-6729 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the erythromycin-6729 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

flucloxacillin-6507 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the flucloxacillin-6507 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bemegride-6668 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bemegride-6668 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

azacyclonol-6298 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the azacyclonol-6298 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxolamine-6624 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxolamine-6624 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

vigabatrin-6314 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the vigabatrin-6314 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

azapropazone-6522 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the azapropazone-6522 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

erastin-6412 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the erastin-6412 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

erastin-6417 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the erastin-6417 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

lobeline-6258 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the lobeline-6258 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

coralyne-6317 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the coralyne-6317 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

pirlindole-6519 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the pirlindole-6519 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

proxymetacaine-6332 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the proxymetacaine-6332 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ketanserin-6649 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ketanserin-6649 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

protriptyline-6338 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the protriptyline-6338 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-674-2179 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-674-2179 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clioquinol-6461 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clioquinol-6461 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

oxybenzone-6309 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the oxybenzone-6309 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ciprofibrate-6138 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ciprofibrate-6138 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

disulfiram-6210 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the disulfiram-6210 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

amphotericin B-6303 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the amphotericin B-6303 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ergocalciferol-6746 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ergocalciferol-6746 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

monobenzone-6713 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the monobenzone-6713 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ranitidine-6324 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ranitidine-6324 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

piretanide-6144 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the piretanide-6144 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

amrinone-6826 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the amrinone-6826 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cefuroxime-6088 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cefuroxime-6088 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

orlistat-6383 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the orlistat-6383 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

orlistat-6388 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the orlistat-6388 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

ifosfamide-6279 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the ifosfamide-6279 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PF-01378883-00-6363 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PF-01378883-00-6363 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

PF-01378883-00-6368 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the PF-01378883-00-6368 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

gliquidone-6004 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the gliquidone-6004 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dexamethasone-6271 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dexamethasone-6271 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bezafibrate-6653 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bezafibrate-6653 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

midodrine-6804 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the midodrine-6804 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

dorzolamide-6142 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the dorzolamide-6142 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

bromopride-6037 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the bromopride-6037 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

atropine oxide-6812 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the atropine oxide-6812 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

clotrimazole-6207 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the clotrimazole-6207 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

terfenadine-6823 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the terfenadine-6823 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

primidone-6723 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the primidone-6723 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

(-)-isoprenaline-6149 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the (-)-isoprenaline-6149 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

0225151-0000-6389 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 0225151-0000-6389 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

0225151-0000-6384 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 0225151-0000-6384 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

betazole-6344 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the betazole-6344 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

valproic acid-6168 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the valproic acid-6168 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

cefapirin-6790 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the cefapirin-6790 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

etanidazole-6211 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the etanidazole-6211 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

tetrahydroalstonine-6209 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the tetrahydroalstonine-6209 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

monastrol-605 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the monastrol-605 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

prochlorperazine-6975 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the prochlorperazine-6975 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

meglumine-6685 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the meglumine-6685 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

propidium iodide-6104 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the propidium iodide-6104 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

metolazone-6292 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the metolazone-6292 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

sulfabenzamide-6634 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the sulfabenzamide-6634 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-665-4704 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-665-4704 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

CP-645525-01-7515 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the CP-645525-01-7515 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

zidovudine-6733 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the zidovudine-6733 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

haloperidol-6963 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the haloperidol-6963 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

haloperidol-6960 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the haloperidol-6960 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

nomegestrol-6525 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the nomegestrol-6525 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

trifluoperazine-6341 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the trifluoperazine-6341 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Prestwick-674-3614 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the Prestwick-674-3614 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

proxymetacaine-6492 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the proxymetacaine-6492 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

valproic acid-629 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the valproic acid-629 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

STOCK1N-35874-6583 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the STOCK1N-35874-6583 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.