Name

blind vision; blindness; retinal diseases; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; retinal diseases; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness; corneal diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; corneal diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness; choroidal neovascularization; macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blind vision; blindness; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blind vision; blindness Gene Set

From GAD Gene-Disease Associations

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

blindness; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

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

retinal degeneration; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

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

retinal dystrophies; retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

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

colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

night blindness; retinal diseases Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

color vision defects; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blindness; retinal degeneration Gene Set

From GAD Gene-Disease Associations

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

arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Retinitis pigmentosa 20 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 42 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 42 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 60 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 60 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis Pigmentosa 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis Pigmentosa 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 69 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 69 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 68 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 68 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 67 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 67 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 66 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 66 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 64 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 64 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 62 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 62 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 37 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 37 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 70 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 70 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 41 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 40 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 40 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 43 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 43 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 44 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 44 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 46 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 46 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 56 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 56 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 54 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 54 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 51 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 51 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 50 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 50 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 58 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 58 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 59 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 59 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 36 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 36 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 26 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 25 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 33 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 33 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 35 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 35 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis pigmentosa 38 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis pigmentosa 38 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis Pigmentosa 37 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 37 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 31 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 31 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 35 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 35 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 25 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 25 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 7 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 26 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 26 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 32 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 32 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 33 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 33 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 36 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 36 from the curated CTD Gene-Disease Associations dataset.

Posterior column ataxia with retinitis pigmentosa Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Posterior column ataxia with retinitis pigmentosa from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 42 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 42 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 11 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 14 Gene Set

From CTD Gene-Disease Associations

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

Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 29 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 29 from the curated CTD Gene-Disease Associations dataset.

Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 18 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 18 from the curated CTD Gene-Disease Associations dataset.

RETINITIS PIGMENTOSA 50 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINITIS PIGMENTOSA 50 from the curated CTD Gene-Disease Associations dataset.

RETINITIS PIGMENTOSA 56 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINITIS PIGMENTOSA 56 from the curated CTD Gene-Disease Associations dataset.

RETINITIS PIGMENTOSA 57 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINITIS PIGMENTOSA 57 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 9 Gene Set

From CTD Gene-Disease Associations

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

RETINITIS PIGMENTOSA 55 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINITIS PIGMENTOSA 55 from the curated CTD Gene-Disease Associations dataset.

RETINITIS PIGMENTOSA 51 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINITIS PIGMENTOSA 51 from the curated CTD Gene-Disease Associations dataset.

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 34 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 34 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 19 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 19 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, Y-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, Y-Linked from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 12 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 13 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 17 from the curated CTD Gene-Disease Associations dataset.

RETINITIS PIGMENTOSA 54 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINITIS PIGMENTOSA 54 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 2 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 3 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 4 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 6 Gene Set

From CTD Gene-Disease Associations

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

Retinitis pigmentosa 1 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 30 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 30 from the curated CTD Gene-Disease Associations dataset.

RETINITIS PIGMENTOSA 58 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINITIS PIGMENTOSA 58 from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa 10 Gene Set

From CTD Gene-Disease Associations

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

Retinitis Pigmentosa 41 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa 41 from the curated CTD Gene-Disease Associations dataset.

retinitis pigmentosa Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinitis pigmentosa Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dominant retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dominant retinitis pigmentosa 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.

autosomal-dominant retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

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

retinitis pigmentosa; usher syndrome Gene Set

From GAD Gene-Disease Associations

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

retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

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

recessive retinitis pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recessive retinitis pigmentosa 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.

retinitis pigmentosa. Gene Set

From GAD Gene-Disease Associations

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

Retinitis Pigmentosa_Retina_GSE128 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Retinitis Pigmentosa_Retina_GSE128 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

retinitis pigmentosa Gene Set

From HPO Gene-Disease Associations

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

retinitis pigmentosa inversa Gene Set

From HPO Gene-Disease Associations

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

Retinitis Pigmentosa Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

retinitis pigmentosa 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa 67 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa 67 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa 66 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa 66 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa-40 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa-40 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, cataract, retinitis pigmentosa, and sperm abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, cataract, retinitis pigmentosa, and sperm abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, juvenile, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, juvenile, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 70 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 70 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 56 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 56 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 57 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 57 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 54 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 54 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 58 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 58 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 59 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 59 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 31 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 31 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 33 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 33 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 34 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 35 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 35 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 36 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 36 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 37 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 37 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 38 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 38 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 39 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 39 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa-12, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa-12, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 4, autosomal dominant or recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 4, autosomal dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa 51 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa 51 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa 55 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa 55 phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, posterior column, with retinitis pigmentosa Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, posterior column, with retinitis pigmentosa phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa-50 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa-50 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 7, digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 7, digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, concentric Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, concentric phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 7 and digenic Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 7 and digenic phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, y-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, y-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, juvenile Gene Set

From OMIM Gene-Disease Associations

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

retinitis pigmentosa 69 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 69 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 68 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 68 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 65 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 65 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 64 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 64 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 63 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 63 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 62 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 62 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 61 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 61 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 60 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 60 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 49 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 49 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 48 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 48 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 44 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 44 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 47 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 47 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 22 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 22 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 29 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 29 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 28 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinitis pigmentosa, x-linked recessive, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinitis pigmentosa, x-linked recessive, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 43 Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 43 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease retinitis pigmentosa from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

eye diseases; retinal diseases Gene Set

From GAD Gene-Disease Associations

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

choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Yemenite deaf-blind hypopigmentation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Yemenite deaf-blind hypopigmentation syndrome from the curated CTD Gene-Disease Associations dataset.

blind loop syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blind Gene Set

From GeneRIF Biological Term Annotations

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

blind ureter Gene Set

From MPO Gene-Phenotype Associations

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

blind uterus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the blind uterus phenotype in transgenic mice from the MPO 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.

activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal neovascularization; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal artery occlusion; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD 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.

gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; kidney diseases; lung diseases; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; gastrointestinal diseases; hematologic diseases; kidney diseases; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic liver diseases; alcoholism; liver diseases; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; infant, premature, diseases; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; infant, premature, diseases; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Vision Disorders Gene Set

From CTD Gene-Disease Associations

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

Color Vision Defects Gene Set

From CTD Gene-Disease Associations

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

Vision, Low Gene Set

From CTD Gene-Disease Associations

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

binocular vision disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

defective colour vision Gene Set

From GAD Gene-Disease Associations

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

glaucoma, open-angle; vision disorders Gene Set

From GAD Gene-Disease Associations

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

macular degeneration; vision, low Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macular degeneration; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; giant cell arteritis; polymyalgia rheumatica; stroke; temporal arteritis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

optic atrophy, hereditary, leber; vision disorders Gene Set

From GAD Gene-Disease Associations

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

vision Gene Set

From GAD High Level Gene-Disease Associations

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

vision Gene Set

From GeneRIF Biological Term Annotations

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

abnormality of vision Gene Set

From HPO Gene-Disease Associations

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

abnormality of binocular vision Gene Set

From HPO Gene-Disease Associations

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

abnormality of vision evoked potentials Gene Set

From HPO Gene-Disease Associations

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

abnormality of color vision Gene Set

From HPO Gene-Disease Associations

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

decreased central vision Gene Set

From HPO Gene-Disease Associations

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

blurred vision Gene Set

From HPO Gene-Disease Associations

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

hemianopic blurring of vision Gene Set

From HPO Gene-Disease Associations

genes associated with the hemianopic blurring of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Vision Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Vision Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Mesopic Vision Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Color Vision Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Color Vision Defects Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Vision, Low Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal vision Gene Set

From MPO Gene-Phenotype Associations

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

vision/eye phenotype Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vision/eye phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

The canonical retinoid cycle in rods (twilight vision) Gene Set

From Reactome Pathways

proteins participating in the The canonical retinoid cycle in rods (twilight vision) pathway from the Reactome Pathways dataset.

The retinoid cycle in cones (daylight vision) Gene Set

From Reactome Pathways

proteins participating in the The retinoid cycle in cones (daylight vision) pathway from the Reactome Pathways dataset.

Retinal Diseases Gene Set

From CTD Gene-Disease Associations

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

hypertension, renal; hypertrophy, left ventricular; retinal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, renal; hypertrophy, left ventricular; retinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal diseases Gene Set

From GAD Gene-Disease Associations

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

diseases in twins; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

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

hypertension; retinal diseases Gene Set

From GAD Gene-Disease Associations

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

Retinal Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Congenital stationary night blindness, autosomal dominant 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, autosomal dominant 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.

Blindness, Cortical Gene Set

From CTD Gene-Disease Associations

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

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.

Night Blindness Gene Set

From CTD Gene-Disease Associations

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

Blindness Gene Set

From CTD Gene-Disease Associations

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

Night blindness, congenital stationary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night blindness, congenital stationary from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A from the curated CTD Gene-Disease Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A from the curated CTD Gene-Disease Associations dataset.

congenital stationary night blindness Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease congenital stationary night blindness from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

night blindness Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

red color blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cortical blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

night blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hereditary night blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital stationary night blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

color blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

red-green color blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blue color blindness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

blindness; trachoma Gene Set

From GAD Gene-Disease Associations

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

blindness; optic atrophy, hereditary, leber Gene Set

From GAD Gene-Disease Associations

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

blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blindness; diabetes mellitus, type 1; diabetes mellitus, type 2; diabetic retinopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blindness Gene Set

From GeneRIF Biological Term Annotations

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

night blindness Gene Set

From HPO Gene-Disease Associations

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

congenital blindness Gene Set

From HPO Gene-Disease Associations

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

blindness Gene Set

From HPO Gene-Disease Associations

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

congenital stationary night blindness Gene Set

From HPO Gene-Disease Associations

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

adult-onset night blindness Gene Set

From HPO Gene-Disease Associations

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

progressive night blindness Gene Set

From HPO Gene-Disease Associations

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

Night Blindness Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Blindness Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

blindness Gene Set

From MPO Gene-Phenotype Associations

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

night blindness, congenital stationary, autosomal dominant 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary, autosomal dominant 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1f, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1f, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1b, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1b, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1c, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1c, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary, autosomal dominant 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1a, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (incomplete), 2b, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (incomplete), 2b, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1e, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1e, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1d, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1d, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (incomplete), 2a, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (incomplete), 2a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiovascular diseases; carotid artery diseases; Gene Set

From GAD Gene-Disease Associations

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

eye diseases; sarcoidosis; skin diseases Gene Set

From GAD Gene-Disease Associations

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

eye diseases; hypersensitivity; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases; hypersensitivity; respiratory tract diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

duodenal diseases; helicobacter infections; stomach diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease duodenal diseases; helicobacter infections; stomach diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, x-linked; kidney diseases; oculocerebrorenal syndrome Gene Set

From GAD Gene-Disease Associations

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

crohn disease; crohn's disease; duodenal diseases; stomach diseases Gene Set

From GAD Gene-Disease Associations

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

acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic liver diseases; carcinoma, hepatocellular; lcc - liver cell carcinoma; liver diseases, alcoholic; liver neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic liver diseases; carcinoma, hepatocellular; lcc - liver cell carcinoma; liver diseases, alcoholic; liver neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic liver diseases; alcoholism; liver cirrhosis, alcoholic; liver diseases, alcoholic; pancreatitis, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic liver diseases; alcoholism; liver cirrhosis, alcoholic; liver diseases, alcoholic; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenoleukodystrophy; demyelinating diseases; metabolic diseases Gene Set

From GAD Gene-Disease Associations

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

apoplexy; cardiovascular diseases; ischemia; stroke; vascular diseases Gene Set

From GAD Gene-Disease Associations

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

carotid artery diseases; vascular diseases Gene Set

From GAD Gene-Disease Associations

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

diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies Gene Set

From GAD Gene-Disease Associations

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

alcoholic liver diseases; alcoholism; liver diseases, alcoholic; pancreatitis, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic liver diseases; alcoholism; liver diseases, alcoholic; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; genetic diseases, x-linked; nystagmus, congenital; nystagmus, pathologic; strabismus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic polyps; gastrointestinal diseases; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic polyps; gastrointestinal diseases; inflammatory bowel disease, nos; inflammatory bowel diseases; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic liver diseases; fatty liver; iron overload; liver cirrhosis; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic liver diseases; fatty liver; iron overload; liver cirrhosis; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; autoimmune diseases; lupus erythematosus, systemic; rheumatic diseases; rheumatism; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; autoimmune diseases; lupus erythematosus, systemic; rheumatic diseases; rheumatism; rheumatoid arthritis; sjogren's syndrome; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal diseases; hypoxia-ischemia, brain; infant, newborn, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anus diseases; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

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

alcoholic liver diseases; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

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

occupational diseases; respiratory tract diseases Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

albuminuria; cardiovascular diseases; diabetes mellitus; hypertension; kidney diseases; renal insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease albuminuria; cardiovascular diseases; diabetes mellitus; hypertension; kidney diseases; renal insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic liver diseases; hemochromatosis; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

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

erythema; rare diseases; skin diseases Gene Set

From GAD Gene-Disease Associations

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

apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; arterial occlusive diseases; atherosclerosis; brain ischemia; carotid artery diseases; embolism; ischemic attack, transient; stroke; transient ischemic attack in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; diabetes mellitus; endocrine system diseases; kidney failure, chronic; urologic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; diabetes mellitus; endocrine system diseases; kidney failure, chronic; urologic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

addison disease; autoimmune diseases; graves disease; hashimoto disease; thyroid diseases Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; diabetes mellitus, type 2; kidney diseases Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic diseases; crohn disease; ileal diseases Gene Set

From GAD Gene-Disease Associations

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

aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemochromatosis; joint diseases; rheumatic diseases; rheumatism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; joint diseases; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; macular degeneration; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c, chronic; liver diseases; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; rheumatic diseases; rheumatism Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; thyroid diseases Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; carotid artery diseases; cerebrovascular disorders; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; carotid artery diseases; cerebrovascular disorders; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; diabetes mellitus; kidney diseases; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; diabetes mellitus; kidney diseases; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; skin diseases, vesiculobullous Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; diabetes complications; myocardial infarction; peripheral arterial disease; peripheral arterial diseases Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; carotid artery diseases; coronary disease; coronary heart disease; coronary restenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery diseases; hypertension; kidney diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery diseases; hypertension; kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cardiovascular diseases; carotid artery diseases; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

choroid diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; intermittent claudication; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; intermittent claudication; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroid diseases; peripheral vascular diseases; vitreous hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; peripheral vascular diseases; vitreous hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

heart diseases; hyperplasia; liver diseases; telangiectasia, hereditary hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart diseases; hyperplasia; liver diseases; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; skin diseases, genetic; vitiligo Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; kidney diseases Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; metabolic diseases; obesity Gene Set

From GAD Gene-Disease Associations

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

alcoholic liver diseases; alcoholism; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

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

aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic diseases; autoimmune diseases; chorea; choreatic disorders; myocarditis; rheumatic heart disease; streptococcal infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; delayed graft function; kidney diseases; postoperative complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; delayed graft function; kidney diseases; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic liver diseases; alcoholism; liver diseases, alcoholic; pancreatitis, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic liver diseases; alcoholism; liver diseases, alcoholic; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; liver diseases; syndrome Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain ischemia; cardiovascular diseases; coronary disease; peripheral vascular diseases; stroke; thrombosis 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.

cardiovascular diseases; cerebral arterial diseases; coronary disease; hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

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

albuminuria; cardiovascular diseases; diabetes mellitus, type 2; hypertension; kidney diseases Gene Set

From GAD Gene-Disease Associations

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

asymptomatic diseases; cyst; cysts; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asymptomatic diseases; cyst; cysts; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; brain ischemia; coronary disease; hyperhomocysteinemia; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arteriosclerosis; carotid artery diseases; hyperlipoproteinemia type i; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; carotid artery diseases; hyperlipoproteinemia type i; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

fibrosis; hepatitis c, chronic; liver diseases; liver diseases, alcoholic Gene Set

From GAD Gene-Disease Associations

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

choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic aneurysm, abdominal; aortic diseases; arterial occlusive diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; diabetes complications; heart diseases; hemochromatosis; iron overload; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; diabetes complications; heart diseases; hemochromatosis; iron overload; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; chagas disease; communicable diseases; dengue; leishmaniasis, cutaneous; myasthenia gravis; pemphigus; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chagas disease; communicable diseases; dengue; leishmaniasis, cutaneous; myasthenia gravis; pemphigus; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dementia; neurodegenerative diseases; prion diseases Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; lung diseases; neoplasms Gene Set

From GAD Gene-Disease Associations

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

Dermatopathia pigmentosa reticularis Gene Set

From CTD Gene-Disease Associations

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

urticaria pigmentosa Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

epilepsy; stevens-johnson syndrome; urticaria pigmentosa Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; stevens-johnson syndrome; urticaria pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pigmentosa Gene Set

From GeneRIF Biological Term Annotations

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

pigmentosaassociated Gene Set

From GeneRIF Biological Term Annotations

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

pigmentosacausing Gene Set

From GeneRIF Biological Term Annotations

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

Urticaria Pigmentosa Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

dermatopathia pigmentosa reticularis Gene Set

From OMIM Gene-Disease Associations

genes associated with the dermatopathia pigmentosa reticularis phenotype from the curated OMIM Gene-Disease Associations dataset.

Retinitis punctata albescens Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinitis punctata albescens phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinitis Gene Set

From CTD Gene-Disease Associations

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

retinitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv; cytomegalovirus retinitis Gene Set

From GAD Gene-Disease Associations

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

aids-related opportunistic infections; cytomegalovirus retinitis; encephalomyelitis; hiv infections; hypersensitivity; mycobacterium avium-intracellulare infection; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aids-related opportunistic infections; cytomegalovirus retinitis; encephalomyelitis; hiv infections; hypersensitivity; mycobacterium avium-intracellulare infection; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinitis punctata albescens Gene Set

From GAD Gene-Disease Associations

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

acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; aids-related opportunistic infections; cytomegalovirus retinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinitis Gene Set

From GeneRIF Biological Term Annotations

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

Cytomegalovirus Retinitis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

retinitis punctata albescens Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis punctata albescens phenotype from the curated OMIM Gene-Disease Associations 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.

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.

Rhegmatogenous retinal detachment, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rhegmatogenous retinal detachment, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal degeneration, autosomal recessive, clumped pigment type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal degeneration, autosomal recessive, clumped pigment type 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.

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.

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.

retinal dimer Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical retinal dimer from the curated CTD Gene-Chemical Interactions dataset.

9-cis-retinal Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 9-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.

13-cis-retinal Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 13-cis-retinal from the curated CTD Gene-Chemical Interactions 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 Detachment Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Detachment 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.

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.

Retinal Artery Occlusion Gene Set

From CTD Gene-Disease Associations

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

Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy 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.

Retinal Dystrophies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Dystrophies 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.

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.

Retinal Degeneration Gene Set

From CTD Gene-Disease Associations

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

Retinal Vein Occlusion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Vein Occlusion 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.

RETINAL DYSPLASIA, PRIMARY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY 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.

Retinal Telangiectasis Gene Set

From CTD Gene-Disease Associations

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

Retinal Nonattachment, Nonsyndromic Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Nonattachment, Nonsyndromic Congenital from the curated CTD Gene-Disease Associations dataset.

Retinal Hemorrhage Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Hemorrhage 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.

Late-Onset Retinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Late-Onset Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.

Retinal Vein Gene Set

From dbGAP Gene-Trait Associations

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

retinal cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal degeneration Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal cell cancer Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal vascular disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

retinal degeneration Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

retinal disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

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

retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vein occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal microaneurysm Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

peripheral retinal degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal telangiectasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vasculitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

macular retinal edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease macular retinal edema 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.

retinal drusen Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vascular occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal edema Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

abnormal retinal correspondence Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal perforation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

acute retinal necrosis syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal ischemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal vascular disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

branch retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central retinal artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal cell cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal hemangioblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

central retinal vein occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

retinal detachment Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

diabetes complications; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

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

cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebrovascular disorders; coronary disease; coronary heart disease; diabetes mellitus; hypercholesterolemia; hyperhomocysteinemia; hypertension; retinal vein occlusion; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

branch retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

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

arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arteriosclerosis; hyperhomocysteinemia; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal function Gene Set

From GAD Gene-Disease Associations

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

adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein Gene Set

From GAD Gene-Disease Associations

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

geographic atrophy; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal degeneration Gene Set

From GAD Gene-Disease Associations

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

hearing loss/deafness; retinal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; retinal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; retinal vein occlusion; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal vein occlusion; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroidal neovascularization; macular degeneration; retinal drusen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroidal neovascularization; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; retinal vascular occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal detachment; vitreoretinopathy, proliferative Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal detachment; vitreoretinopathy, proliferative in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vascular occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal detachment Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

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

hypertension; retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

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

behcet syndrome; retinal vasculitis Gene Set

From GAD Gene-Disease Associations

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

retinal vein occlusion; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein thrombosis Gene Set

From GAD Gene-Disease Associations

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

behcet's disease; retinal vasculitis; uveitis Gene Set

From GAD Gene-Disease Associations

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

retinal artery occlusion Gene Set

From GAD Gene-Disease Associations

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

retinal neoplasms; retinoblastoma Gene Set

From GAD Gene-Disease Associations

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

retinal vascular occlusive disease Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

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

neovascularization, pathologic; retinal vasculitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neovascularization, pathologic; retinal vasculitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

atherosclerosis; inflammation; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hyperlipidemias; hypertension; retinal vein occlusion; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease choroidal neovascularization; retinal drusen; wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; retinal vein occlusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

retinal Gene Set

From GeneRIF Biological Term Annotations

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

regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

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

retinal bipolar neuron differentiation Gene Set

From GO Biological Process Annotations

genes participating in the retinal bipolar neuron differentiation biological process from the curated GO Biological Process Annotations dataset.

retinal pigment epithelium development Gene Set

From GO Biological Process Annotations

genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations dataset.

retinal blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

retinal rod cell development Gene Set

From GO Biological Process Annotations

genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations dataset.

retinal metabolic process Gene Set

From GO Biological Process Annotations

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

retinal cell apoptotic process Gene Set

From GO Biological Process Annotations

genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations dataset.

regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retinal cone cell development Gene Set

From GO Biological Process Annotations

genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations dataset.

retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

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

positive regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal cell programmed cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of retinal ganglion cell axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations dataset.

retinal rod cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations dataset.

retinal dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

retinal isomerase activity Gene Set

From GO Molecular Function Annotations

genes performing the retinal isomerase activity molecular function from the curated GO Molecular Function Annotations dataset.

all-trans retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

11-cis retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

retinal binding Gene Set

From GO Molecular Function Annotations

genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations dataset.

all-trans-retinal Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the all-trans-retinal ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Retinal vascular caliber Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Retinal vascular caliber phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Rhegmatogenous retinal detachment Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Rhegmatogenous retinal detachment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

retinal degeneration Gene Set

From GWASdb SNP-Disease Associations

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

retinal disease Gene Set

From GWASdb SNP-Disease Associations

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

retinal detachment Gene Set

From GWASdb SNP-Disease Associations

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

retinal vascular disease Gene Set

From GWASdb SNP-Disease Associations

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

abnormality of retinal arteries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

retinal coloboma Gene Set

From GWASdb SNP-Phenotype Associations

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

rhegmatogenous retinal detachment Gene Set

From GWASdb SNP-Phenotype Associations

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

retinal detachment Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the retinal vasculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

4-OH-Retinal Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4-OH-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.

Retinal Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.

9-cis-Retinal Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 9-cis-Retinal metabolite from the curated HMDB Metabolites of Enzymes dataset.

retinal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal hypoplasia 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.

retinal dysplasia Gene Set

From HPO Gene-Disease Associations

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

retinal striation Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal atrophy Gene Set

From HPO Gene-Disease Associations

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

lacunar retinal depigmentation Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

focal retinal infarction Gene Set

From HPO Gene-Disease Associations

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

exudative retinal detachment Gene Set

From HPO Gene-Disease Associations

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

tractional retinal detachment Gene Set

From HPO Gene-Disease Associations

genes associated with the tractional retinal detachment 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.

rarefaction of retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

abnormal retinal folds Gene Set

From HPO Gene-Disease Associations

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

large hyperpigmented retinal spots Gene Set

From HPO Gene-Disease Associations

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

retinal telangiectasia Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal pigmentation abnormalities Gene Set

From HPO Gene-Disease Associations

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

absent retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

depigmented lesions of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

genes associated with the depigmented lesions of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

achromatic retinal patches Gene Set

From HPO Gene-Disease Associations

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

retinal calcification Gene Set

From HPO Gene-Disease Associations

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

retinal vascular malformation Gene Set

From HPO Gene-Disease Associations

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

retinal neoplasm Gene Set

From HPO Gene-Disease Associations

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

retinal vascular tortuosity Gene Set

From HPO Gene-Disease Associations

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

retinal detachment Gene Set

From HPO Gene-Disease Associations

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

retinal flecks Gene Set

From HPO Gene-Disease Associations

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

retinal arteriolar constriction Gene Set

From HPO Gene-Disease Associations

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

peripheral retinal avascularization Gene Set

From HPO Gene-Disease Associations

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

retinal pigment epithelial atrophy Gene Set

From HPO Gene-Disease Associations

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

retinal nonattachment Gene Set

From HPO Gene-Disease Associations

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

decreased retinal pigmentation with dispersion Gene Set

From HPO Gene-Disease Associations

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

retinal malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal malformation 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.

falciform retinal fold Gene Set

From HPO Gene-Disease Associations

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

congenital hypertrophy of retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital hypertrophy of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

retinal hemorrhage Gene Set

From HPO Gene-Disease Associations

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

pigmentary retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

loss of retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

pigmentary retinal deposits Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retinal vasculature Gene Set

From HPO Gene-Disease Associations

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

macular retinal pigment epithelial mottling Gene Set

From HPO Gene-Disease Associations

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

retinal arteriolar tortuosity Gene Set

From HPO Gene-Disease Associations

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

abnormal retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

retinal arteriolar occlusion Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal arteriolar occlusion 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.

abnormality of retinal arteries Gene Set

From HPO Gene-Disease Associations

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

rhegmatogenous retinal detachment Gene Set

From HPO Gene-Disease Associations

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

honeycomb retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

hypermyelinated retinal fibers Gene Set

From HPO Gene-Disease Associations

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

retinal coloboma Gene Set

From HPO Gene-Disease Associations

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

retinal exudate Gene Set

From HPO Gene-Disease Associations

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

retinal hamartoma Gene Set

From HPO Gene-Disease Associations

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

cystic retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

progressive retinal degeneration Gene Set

From HPO Gene-Disease Associations

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

retinal vascular proliferation Gene Set

From HPO Gene-Disease Associations

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

attenuation of retinal blood vessels Gene Set

From HPO Gene-Disease Associations

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

peripheral traction retinal detachment Gene Set

From HPO Gene-Disease Associations

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

retinal hemangioblastoma Gene Set

From HPO Gene-Disease Associations

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

retinal atrophy Gene Set

From HPO Gene-Disease Associations

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

Retinal Detachment Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Artery Occlusion Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Dystrophies Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Degeneration Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Vein Occlusion Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Drusen Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Vasculitis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Neovascularization Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Perforations Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal Hemorrhage Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Retinal pigment epithelium GPCR Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal pigment epithelium GPCR protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal-specific ATP-binding cassette transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal-specific ATP-binding cassette transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal protein C2orf71 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal protein C2orf71 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal rod rhodopsin-sensitive cGMP 3', 5'-cyclic phosphodiesterase, delta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal cGMP phosphodiesterase, gamma subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal cGMP phosphodiesterase, gamma subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Visual pigments (opsins) retinal binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Visual pigments (opsins) retinal binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal degeneration protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal degeneration protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal retinal photoreceptor layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal fibrosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal inner nuclear layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal melanocyte morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal rod cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal ganglion cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal ganglion cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal inner plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal neuronal layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal neuronal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal outer nuclear layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal outer nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal rod cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal rod cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thick retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thick retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal cone cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal degeneration Gene Set

From MPO Gene-Phenotype Associations

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

retinal pigment epithelium atrophy Gene Set

From MPO Gene-Phenotype Associations

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

disorganized retinal layers Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal layers phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal photoreceptor morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased retinal ganglion cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal pigment epithelium hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal pigment epithelium hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal progenitor cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal deposits Gene Set

From MPO Gene-Phenotype Associations

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

abnormal induced retinal neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal induced retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal ganglion layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal ganglion layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased retinal photoreceptor cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal photoreceptor cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal ischemia Gene Set

From MPO Gene-Phenotype Associations

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

retinal outer nuclear layer degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal outer nuclear layer degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal rod cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal rod cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal detachment Gene Set

From MPO Gene-Phenotype Associations

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

retinal cone cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal cone cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal gliosis Gene Set

From MPO Gene-Phenotype Associations

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

thin retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal apoptosis Gene Set

From MPO Gene-Phenotype Associations

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

thin retinal inner nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal vasculature morphology Gene Set

From MPO Gene-Phenotype Associations

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

retinal ganglion cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retinal ganglion cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal ganglion cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal hemorrhage Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal outer plexiform layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal ganglion cell Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal ganglion cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal cone cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal cone cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal outer nuclear layer thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal outer nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal spots Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal blood vessel pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal inner plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased retinal rod cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased retinal rod cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

decreased susceptibility to induced retinal damage Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal nerve fiber layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal rod cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retinal photoreceptor degeneration Gene Set

From MPO Gene-Phenotype Associations

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

disorganized retinal outer plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal outer nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal pigment epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal pigment epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased retinal cone cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal outer plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal inner plexiform layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal inner plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal inner nuclear layer thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal inner nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal inner nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

retinal neovascularization Gene Set

From MPO Gene-Phenotype Associations

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

disorganized retinal ganglion layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal melanin granule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{retinal disease in usher syndrome type iia, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {retinal disease in usher syndrome type iia, modifier of} 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.

retinal dystrophy, early-onset severe Gene Set

From OMIM Gene-Disease Associations

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

retinal degeneration, late-onset, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

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

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 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.

?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.

retinal nonattachment, nonsyndromic congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal nonattachment, nonsyndromic congenital 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.

retinal arterial macroaneurysm with supravalvular pulmonic stenosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal arterial macroaneurysm with supravalvular pulmonic stenosis 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.

infantile cerebellar-retinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal degeneration, autosomal recessive, clumped pigment type Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal degeneration, autosomal recessive, clumped pigment type 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.

vasculopathy, retinal, with cerebral leukodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the vasculopathy, retinal, with cerebral leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Biosynthesis of A2E, implicated in retinal degradation Gene Set

From Reactome Pathways

proteins participating in the Biosynthesis of A2E, implicated in retinal degradation pathway from the Reactome Pathways dataset.

retinal rod Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue retinal pigment epithelium from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

retinal cone Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

retinal microvascular endothelial cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal ganglion cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal pigment epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal stem cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal cone Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal rod Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retinal ganglion cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Neural retinal development(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Neural retinal development(Mus musculus) pathway from the Wikipathways Pathways dataset.

Mitochondrial diseases Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial diseases phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Liver Diseases, Parasitic Gene Set

From CTD Gene-Disease Associations

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

Stomach Diseases Gene Set

From CTD Gene-Disease Associations

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

Carotid Artery Diseases Gene Set

From CTD Gene-Disease Associations

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

Neuromuscular Diseases Gene Set

From CTD Gene-Disease Associations

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

Bile Duct Diseases Gene Set

From CTD Gene-Disease Associations

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

Virus Diseases Gene Set

From CTD Gene-Disease Associations

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

Maxillary Diseases Gene Set

From CTD Gene-Disease Associations

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

Rheumatic Diseases Gene Set

From CTD Gene-Disease Associations

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

Thoracic Diseases Gene Set

From CTD Gene-Disease Associations

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

Foodborne Diseases Gene Set

From CTD Gene-Disease Associations

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

Eye Diseases, Hereditary Gene Set

From CTD Gene-Disease Associations

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

Prion Diseases Gene Set

From CTD Gene-Disease Associations

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

Skin Diseases Gene Set

From CTD Gene-Disease Associations

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

Lacrimal Apparatus Diseases Gene Set

From CTD Gene-Disease Associations

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

Placenta Diseases Gene Set

From CTD Gene-Disease Associations

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

Laryngeal Diseases Gene Set

From CTD Gene-Disease Associations

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

Lung Diseases, Interstitial Gene Set

From CTD Gene-Disease Associations

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

Vestibular Diseases Gene Set

From CTD Gene-Disease Associations

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

Kidney Diseases Gene Set

From CTD Gene-Disease Associations

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

Hair Diseases Gene Set

From CTD Gene-Disease Associations

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

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Infant, Newborn, Diseases Gene Set

From CTD Gene-Disease Associations

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

Periodontal Diseases Gene Set

From CTD Gene-Disease Associations

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

Skin Diseases, Vascular Gene Set

From CTD Gene-Disease Associations

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

Uterine Diseases Gene Set

From CTD Gene-Disease Associations

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

Neurodegenerative Diseases Gene Set

From CTD Gene-Disease Associations

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

Male Urogenital Diseases Gene Set

From CTD Gene-Disease Associations

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

Infant, Premature, Diseases Gene Set

From CTD Gene-Disease Associations

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

Bone Marrow Diseases Gene Set

From CTD Gene-Disease Associations

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

Dog Diseases Gene Set

From CTD Gene-Disease Associations

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

Hematologic Diseases Gene Set

From CTD Gene-Disease Associations

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

Pleural Diseases Gene Set

From CTD Gene-Disease Associations

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

Bone Diseases, Metabolic Gene Set

From CTD Gene-Disease Associations

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

Occupational Diseases Gene Set

From CTD Gene-Disease Associations

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

Eyelid Diseases Gene Set

From CTD Gene-Disease Associations

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

Lung Diseases, Obstructive Gene Set

From CTD Gene-Disease Associations

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

Mitochondrial Diseases Gene Set

From CTD Gene-Disease Associations

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

Bone Diseases, Developmental Gene Set

From CTD Gene-Disease Associations

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

Gallbladder Diseases Gene Set

From CTD Gene-Disease Associations

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

Eye Diseases Gene Set

From CTD Gene-Disease Associations

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

Mouth Diseases Gene Set

From CTD Gene-Disease Associations

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

Nail Diseases Gene Set

From CTD Gene-Disease Associations

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

Heart Valve Diseases Gene Set

From CTD Gene-Disease Associations

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

Ovarian Diseases Gene Set

From CTD Gene-Disease Associations

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

Cartilage Diseases Gene Set

From CTD Gene-Disease Associations

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

Ileal Diseases Gene Set

From CTD Gene-Disease Associations

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

Vaginal Diseases Gene Set

From CTD Gene-Disease Associations

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

Lymphatic Diseases Gene Set

From CTD Gene-Disease Associations

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

Autoimmune Diseases of the Nervous System Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Autoimmune Diseases of the Nervous System from the curated CTD Gene-Disease Associations dataset.

Basal Ganglia Diseases Gene Set

From CTD Gene-Disease Associations

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

Peripheral Nervous System Diseases Gene Set

From CTD Gene-Disease Associations

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

Testicular Diseases Gene Set

From CTD Gene-Disease Associations

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

Cranial Nerve Diseases Gene Set

From CTD Gene-Disease Associations

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

Respiratory Tract Diseases Gene Set

From CTD Gene-Disease Associations

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

Adrenal Cortex Diseases Gene Set

From CTD Gene-Disease Associations

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

Demyelinating Diseases Gene Set

From CTD Gene-Disease Associations

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

Arterial Occlusive Diseases Gene Set

From CTD Gene-Disease Associations

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

Hereditary Autoinflammatory Diseases Gene Set

From CTD Gene-Disease Associations

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

Cerebellar Diseases Gene Set

From CTD Gene-Disease Associations

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

Aortic Diseases Gene Set

From CTD Gene-Disease Associations

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

Abducens Nerve Diseases Gene Set

From CTD Gene-Disease Associations

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

Prostatic Diseases Gene Set

From CTD Gene-Disease Associations

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

Niemann-Pick Diseases Gene Set

From CTD Gene-Disease Associations

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

Gastrointestinal Diseases Gene Set

From CTD Gene-Disease Associations

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

Intestinal Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intestinal Diseases 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.

Bone Diseases, Endocrine Gene Set

From CTD Gene-Disease Associations

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

Spinal Cord Diseases Gene Set

From CTD Gene-Disease Associations

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

Stomatognathic Diseases Gene Set

From CTD Gene-Disease Associations

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

Bronchial Diseases Gene Set

From CTD Gene-Disease Associations

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

Peripheral Vascular Diseases Gene Set

From CTD Gene-Disease Associations

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

Central Nervous System Diseases Gene Set

From CTD Gene-Disease Associations

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

Nervous System Diseases Gene Set

From CTD Gene-Disease Associations

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

Autonomic Nervous System Diseases Gene Set

From CTD Gene-Disease Associations

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

Optic Nerve Diseases Gene Set

From CTD Gene-Disease Associations

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

Breast Diseases Gene Set

From CTD Gene-Disease Associations

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

Bone Diseases Gene Set

From CTD Gene-Disease Associations

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

Brain Diseases Gene Set

From CTD Gene-Disease Associations

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

Female Urogenital Diseases Gene Set

From CTD Gene-Disease Associations

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

Autoimmune Diseases Gene Set

From CTD Gene-Disease Associations

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

Genetic Diseases, X-Linked Gene Set

From CTD Gene-Disease Associations

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

Corneal Diseases Gene Set

From CTD Gene-Disease Associations

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

Cardiovascular Diseases Gene Set

From CTD Gene-Disease Associations

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

Pituitary Diseases Gene Set

From CTD Gene-Disease Associations

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

Vascular Diseases Gene Set

From CTD Gene-Disease Associations

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

Urologic Diseases Gene Set

From CTD Gene-Disease Associations

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

Connective Tissue Diseases Gene Set

From CTD Gene-Disease Associations

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

Genetic Diseases, Inborn Gene Set

From CTD Gene-Disease Associations

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

Lung Diseases Gene Set

From CTD Gene-Disease Associations

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

Liver Diseases Gene Set

From CTD Gene-Disease Associations

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

Agricultural Workers' Diseases Gene Set

From CTD Gene-Disease Associations

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

Joint Diseases Gene Set

From CTD Gene-Disease Associations

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

Genital Diseases, Male Gene Set

From CTD Gene-Disease Associations

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

Tick-Borne Diseases Gene Set

From CTD Gene-Disease Associations

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

Adrenal Gland Diseases Gene Set

From CTD Gene-Disease Associations

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

Penile Diseases Gene Set

From CTD Gene-Disease Associations

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

Splenic Diseases Gene Set

From CTD Gene-Disease Associations

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

Myelodysplastic-Myeloproliferative Diseases Gene Set

From CTD Gene-Disease Associations

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

Brain Diseases, Metabolic Gene Set

From CTD Gene-Disease Associations

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

Kidney Diseases, Cystic Gene Set

From CTD Gene-Disease Associations

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

Deficiency Diseases Gene Set

From CTD Gene-Disease Associations

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

Lens Diseases Gene Set

From CTD Gene-Disease Associations

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

Cochlear Diseases Gene Set

From CTD Gene-Disease Associations

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

Fetal Diseases Gene Set

From CTD Gene-Disease Associations

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

X-Linked Combined Immunodeficiency Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-Linked Combined Immunodeficiency Diseases from the curated CTD Gene-Disease Associations dataset.

Immune Complex Diseases Gene Set

From CTD Gene-Disease Associations

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

Polycystic Kidney Diseases Gene Set

From CTD Gene-Disease Associations

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

Urinary Bladder Diseases Gene Set

From CTD Gene-Disease Associations

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

Fish Diseases Gene Set

From CTD Gene-Disease Associations

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

Conjunctival Diseases Gene Set

From CTD Gene-Disease Associations

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

Esophageal Diseases Gene Set

From CTD Gene-Disease Associations

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

Endocrine System Diseases Gene Set

From CTD Gene-Disease Associations

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

Immune System Diseases Gene Set

From CTD Gene-Disease Associations

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

Thyroid Diseases Gene Set

From CTD Gene-Disease Associations

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

Liver Diseases, Alcoholic Gene Set

From CTD Gene-Disease Associations

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

Inflammatory Bowel Diseases Gene Set

From CTD Gene-Disease Associations

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

Metabolic Diseases Gene Set

From CTD Gene-Disease Associations

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

Musculoskeletal Diseases Gene Set

From CTD Gene-Disease Associations

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

Ear Diseases Gene Set

From CTD Gene-Disease Associations

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

Genital Diseases, Female Gene Set

From CTD Gene-Disease Associations

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

Brain Diseases, Metabolic, Inborn Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Brain Diseases, Metabolic, Inborn from the curated CTD Gene-Disease Associations dataset.

Pancreatic Diseases Gene Set

From CTD Gene-Disease Associations

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

Mandibular Diseases Gene Set

From CTD Gene-Disease Associations

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

Heart Diseases Gene Set

From CTD Gene-Disease Associations

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

Carotid Artery Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Gallbladder Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Autoimmune Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Prion Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Cardiovascular Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Kidney Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Vascular Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Inflammatory Bowel Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Intestinal Diseases Gene Set

From dbGAP Gene-Trait Associations

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

Heart Diseases Gene Set

From dbGAP Gene-Trait Associations

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

kidney diseases Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; hepatitis, autoimmune Gene Set

From GAD Gene-Disease Associations

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

behcet syndrome; nervous system diseases; ulcer Gene Set

From GAD Gene-Disease Associations

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

apoplexy; stroke; thrombotic microangiopathies; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; stroke; thrombotic microangiopathies; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases Gene Set

From GAD Gene-Disease Associations

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

tongue diseases Gene Set

From GAD Gene-Disease Associations

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

arthritis, rheumatoid; cardiovascular diseases; obesity Gene Set

From GAD Gene-Disease Associations

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

heart diseases; inflammation; myocardial infarction Gene Set

From GAD Gene-Disease Associations

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

lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung diseases; mycobacterium avium-intracellulare infection; mycobacterium infections, atypical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; macular degeneration Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; ileus; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cystic fibrosis; ileus; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; obesity; overweight Gene Set

From GAD Gene-Disease Associations

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

htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nephritis, interstitial; polycystic kidney diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nephritis, interstitial; polycystic kidney diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; coronary disease; coronary heart disease; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

kidney diseases; postoperative complications Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; biliary cirrhosis; liver cirrhosis, biliary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; biliary cirrhosis; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; cardiovascular diseases; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

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

inflammatory bowel diseases; psoriasis; spondylitis, ankylosing Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory bowel diseases; psoriasis; spondylitis, ankylosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; infarction; ischemia; sickle cell anemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

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

bone marrow diseases; syndrome Gene Set

From GAD Gene-Disease Associations

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

cicatrization; kidney diseases; urinary incontinence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cicatrization; kidney diseases; urinary incontinence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diseases in twins Gene Set

From GAD Gene-Disease Associations

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

nasopharyngeal neoplasms; occupational diseases Gene Set

From GAD Gene-Disease Associations

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

intestinal pseudo-obstruction; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal pseudo-obstruction; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

fetal diseases; hemoglobinopathies Gene Set

From GAD Gene-Disease Associations

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

rheumatic diseases; rheumatism Gene Set

From GAD Gene-Disease Associations

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

kidney failure, chronic; vascular diseases Gene Set

From GAD Gene-Disease Associations

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

acquired immunodeficiency syndrome; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; obesity; virilism Gene Set

From GAD Gene-Disease Associations

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

inflammatory bowel disease, nos; inflammatory bowel diseases; leukopenia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory bowel disease, nos; inflammatory bowel diseases; leukopenia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glycogen storage disease type ii; heart diseases Gene Set

From GAD Gene-Disease Associations

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

peripheral vascular diseases; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; inflammation; neoplasms Gene Set

From GAD Gene-Disease Associations

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

cystic fibrosis; lung diseases Gene Set

From GAD Gene-Disease Associations

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

activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; hyperhomocysteinemia; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; occupational diseases Gene Set

From GAD Gene-Disease Associations

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

complete hearing loss; deafness; vestibular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; vestibular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic ulcerative colitis; colitis, ulcerative; crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; peripheral vascular diseases; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii; peripheral vascular diseases; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; calculi; pancreatitis, chronic; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; calculi; pancreatitis, chronic; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; calcinosis; pancreatitis, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; calcinosis; pancreatitis, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; cardiovascular diseases; inflammation; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

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

graves disease; thyroid diseases Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; meniere disease Gene Set

From GAD Gene-Disease Associations

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

biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease biliary cirrhosis; cholangitis, sclerosing; cystic fibrosis; inflammatory bowel disease, nos; inflammatory bowel diseases; liver cirrhosis, biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; disease susceptibility; skin diseases Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

atherosclerosis, coronary; diabetes, type 1; nephropathy in other diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis, coronary; diabetes, type 1; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; cell transformation, neoplastic; heart diseases; mammary neoplasms; neoplasms, experimental Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; cell transformation, neoplastic; heart diseases; mammary neoplasms; neoplasms, experimental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

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

occupational diseases Gene Set

From GAD Gene-Disease Associations

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

nephropathy in other diseases; cerebrovascular disease Gene Set

From GAD Gene-Disease Associations

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

bone marrow diseases; lupus erythematosus, systemic; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

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

brain ischemia; heart diseases; stroke Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; diabetes mellitus; neoplasms Gene Set

From GAD Gene-Disease Associations

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

graves disease; graves ophthalmopathy; orbital diseases Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; lyme disease Gene Set

From GAD Gene-Disease Associations

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

musculoskeletal diseases Gene Set

From GAD Gene-Disease Associations

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

occupational diseases; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

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

agammaglobulinemia; genetic diseases, x-linked Gene Set

From GAD Gene-Disease Associations

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

urologic diseases Gene Set

From GAD Gene-Disease Associations

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

albuminuria; hypertension; kidney diseases Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; sleep apnea, obstructive Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; dementia; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

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

lung neoplasms; occupational diseases Gene Set

From GAD Gene-Disease Associations

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

henoch-schoenlein purpura; kidney diseases; nephrotic syndrome; proteinuria; purpura, schoenlein-henoch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease henoch-schoenlein purpura; kidney diseases; nephrotic syndrome; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; inflammatory bowel disease, nos; inflammatory bowel diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery diseases Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; myocardial infarction; stroke Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

cardiovascular diseases; ventricular dysfunction, left Gene Set

From GAD Gene-Disease Associations

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