Retinal atrophy

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Results for "Retinal atrophy": 1002 gene sets

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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 atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
muscular atrophy, spinal; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
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.
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 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.
Retinal Pigment Epithelium Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelium Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Pigment Epithelial Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal pigment epithelial atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal pigment epithelial atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
Retinal detachment or retinal break Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment or retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal detachment with retinal break Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment with retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bosch-boonstra-schaaf optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dominant hereditary optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, X-linked 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked myopathy with postural muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic Atrophy Type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital microvillous atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, autosomal recessive 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sveinsson Chorioretinal Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sveinsson Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy, Hereditary, Leber Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy, Jerash type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 1 and deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 5 from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy with respiratory distress 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.
Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrophy from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy from the curated CTD Gene-Disease Associations dataset.
Myopathy, X-Linked, With Postural Muscle Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset.
Costeff optic atrophy syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy polyneuropathy deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
Chorioretinal atrophy, progressive bifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Gyrate Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gyrate Atrophy from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset.
Pigmented Paravenous Chorioretinal Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.
OPTIC ATROPHY 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OPTIC ATROPHY 2 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy, Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrophy of prostate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
primary optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrophy of testis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary choroidal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
olivopontocerebellar atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
survival motor neuron spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gyrate atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
choroidal neovascularization; geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; dementia; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; helicobacter infections; metaplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; geographic atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
posterior cortical atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease posterior cortical atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; helicobacter infections; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; helicobacter infections Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; prenatal exposure delayed effects; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; prenatal exposure delayed effects; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic disc atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease optic disc atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gyrate atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gyrate atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; peptic ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; brain diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; aphasia; atrophy; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; aphasia; atrophy; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gastric atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gastric atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy phenotype Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
alzheimer disease; amnesia; atrophy; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; amnesia; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stomach cancer; stomach atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease stomach cancer; stomach atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; atrophy; brain diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; epilepsy; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy and moderate deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy and moderate deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; helicobacter infections; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; brain atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; huntington disease Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hippocampal atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease hippocampal atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonic disorders; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term atrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
skeletal muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
striated muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
MRI atrophy measures Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the MRI atrophy measures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hippocampal atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hippocampal atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
muscular atrophy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease muscular atrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
motor neuron atrophy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the motor neuron atrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
type 2 muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the type 2 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
levator palpebrae superioris atrophy Gene Set From HPO Gene-Disease Associations genes associated with the levator palpebrae superioris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral white matter atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the corticospinal tracts Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized limb muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
global brain atrophy Gene Set From HPO Gene-Disease Associations genes associated with the global brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
caudate atrophy Gene Set From HPO Gene-Disease Associations genes associated with the caudate atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corpus callosum atrophy Gene Set From HPO Gene-Disease Associations genes associated with the corpus callosum atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tubular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the tubular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thenar muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the thenar muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pontocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
brain atrophy Gene Set From HPO Gene-Disease Associations genes associated with the brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skeletal muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the skeletal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tongue atrophy Gene Set From HPO Gene-Disease Associations genes associated with the tongue atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
olivopontocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the olivopontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic atrophy Gene Set From HPO Gene-Disease Associations genes associated with the optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dermal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the dermal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripapillary chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the frontal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcortical cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse skin atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor neuron atrophy Gene Set From HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pelvic girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pelvic girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
leber optic atrophy Gene Set From HPO Gene-Disease Associations genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral axonal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fundus atrophy Gene Set From HPO Gene-Disease Associations genes associated with the fundus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
scapular muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the scapular muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the cerebrum Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
first dorsal interossei muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the first dorsal interossei muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the brainstem Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the caudate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the caudate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic atrophy from cranial nerve compression Gene Set From HPO Gene-Disease Associations genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
villous atrophy Gene Set From HPO Gene-Disease Associations genes associated with the villous atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
iris atrophy Gene Set From HPO Gene-Disease Associations genes associated with the iris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of alveolar ridges Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the renal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
interosseus muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the interosseus muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
type 1 muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
superior rectus atrophy Gene Set From HPO Gene-Disease Associations genes associated with the superior rectus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
noninflammatory macular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the noninflammatory macular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized cerebral atrophy/hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb-girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the limb-girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
testicular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the testicular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
shoulder girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the shoulder girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmented paravenous chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peroneal muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peroneal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontotemporal cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the frontotemporal cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of the dentate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
quadriceps muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the quadriceps muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the spinocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
temporal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the temporal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy, Hereditary, Leber Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy, Spinal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Geographic Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Geographic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic atrophy 3-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
dentatorubropallidoluysian atrophy Gene Set From KEGG Pathways proteins participating in the dentatorubropallidoluysian atrophy pathway from the KEGG Pathways dataset.
ovary atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ovary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle fiber atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney cortex atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
testicular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the testicular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney collecting duct atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thymus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thymus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
brain atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the brain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sebaceous gland atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
midbrain atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal tubule atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
seminal vesicle atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
meibomian gland atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the meibomian gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
uterus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreatic acinar cell atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
endometrium atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epidermal atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
exocrine pancreas atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spleen atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spleen atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
iris atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the iris atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vagina atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vagina atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to induced muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vulva atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vulva atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreas atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
oviduct atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
external male genitalia atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney medulla atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney papillary atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 6 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 5 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy-4 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, x-linked 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple system atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, x-linked, with postural muscle atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, chronic distal, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, jokela type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset.
sveinsson choreoretinal atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the sveinsson choreoretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
scapuloperoneal spinal muscular atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, late-onset, finkel type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.
dentatorubro-pallidoluysian atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the dentatorubro-pallidoluysian atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
{spinal muscular atrophy, type iii, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy-7 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia, optic atrophy, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
bosch-boonstra-schaaf optic atrophy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 2, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
gyrate atrophy of choroid and retina with or without ornithinemia Gene Set From OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 3 with cataract Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From OMIM Gene-Disease Associations genes associated with the microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, x-linked 3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.
pigmented paravenous chorioretinal atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
?neurodegeneration with optic atrophy, childhood onset Gene Set From OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal and bulbar muscular atrophy of kennedy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy plus syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, congenital nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
{leber optic atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Geographic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Geographic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bulbo-Spinal Atrophy, X-Linked Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bulbo-Spinal Atrophy, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Linear Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Linear Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brain Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Testis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Testis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Olivopontocerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Infantile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Limb Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Limb Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscle Fiber Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Neuron Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcortical Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcortical Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sveinsson Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sveinsson Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Villous Atrophy Of Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Villous Atrophy Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontotemporal Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Cerebral Atrophy/Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Cerebral Atrophy/Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentatorubral-Pallidoluysian Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentatorubral-Pallidoluysian Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy, Disuse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Disuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of The Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Corpus Callosum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral White Matter Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral White Matter Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Prostate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pelvic Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pelvic Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy, Muscular, Spinobulbar Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Muscular, Spinobulbar in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proliferative Inflammatory Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proliferative Inflammatory Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gyrate Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Distal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy/Degeneration Affecting The Brainstem Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy/Degeneration Affecting The Brainstem in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy, Cerebellar Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominant Hereditary Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Hereditary Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Atrophy Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Atrophy Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Tongue Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paravenous Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pigmented Paravenous Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmented Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Cortical Atrophy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Cortical Atrophy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Vagina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urogenital Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urogenital Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroneal Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Atrophy, Progressive Bifocal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy, Progressive Bifocal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Skin Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Skin Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cervical Spinal Cord Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cervical Spinal Cord Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Splenic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Splenic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Atrophy Of Thyroid Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atrophy Of Thyroid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sporadic Olivopontocerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sporadic Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Axonal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Tongue Papillae Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue Papillae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pancreatic Acinar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pancreatic Acinar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Tubular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glaucomatous Atrophy Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leber Optic Atrophy And Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leber Optic Atrophy And Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Seminal Vesicle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Seminal Vesicle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripapillary Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Optic Atrophy Plus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Optic Atrophy Plus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Cortical Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Cortical Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rectus Femoris Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rectus Femoris Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Parietal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Parietal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oculopharyngeal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngeal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Proximal Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Form Of Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Form Of Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonprogressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodontal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Skeletal Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skeletal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foveal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foveal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hippocampal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hippocampal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Muscle Atrophy Due To Neurologic Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Shoulder Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shoulder Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Global Brain Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Global Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Choriocapillaris Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Choriocapillaris Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mucosal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mucosal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Villous Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Villous Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Caudate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Caudate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of Quadriceps Femoris Muscle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Quadriceps Femoris Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Fiber Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurogenic Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurogenic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebral Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of The Dentate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of The Dentate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Corticospinal Tract Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corticospinal Tract Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Purkinje Layer Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Purkinje Layer Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Vermis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Extremity Muscle Atrophy, Lower Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Extremity Muscle Atrophy, Lower in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Caudate Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caudate Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
First Dorsal Interossei Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype First Dorsal Interossei Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thenar Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thenar Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of Alveolar Ridges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Alveolar Ridges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Scapular Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scapular Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intrinsic Hand Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrinsic Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pontocerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tubular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tubular Atrophy Assessment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubular Atrophy Assessment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripapillary Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tibialis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tibialis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fundus Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fundus Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Levator Palpebrae Superioris Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Levator Palpebrae Superioris Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Superior Rectus Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Superior Rectus Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Frontal Lobe Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Frontal Lobe Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axial Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axial Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Spinal Cord Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of Vas Deferens Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Vas Deferens in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Cerebrum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Cerebrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
skeletal muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
striated muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Meibomian gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Meibomian gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
renal glomerulus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
temporal lobe atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the temporal lobe atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
alveolar process atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the alveolar process atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
testicular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the testicular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thymus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spleen atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spleen atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
renal tubule atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pancreatic acinar cell atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lacrimal gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lacrimal gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney cortex atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ovary atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
uterus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the uterus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
external male genitalia atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vulva atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vulva atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vagina atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vagina atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
endometrium atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney collecting duct atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney medulla atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thymus cortex atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus cortex atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle fiber atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebellum atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebellum atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Leydig cell atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Leydig cell atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina pigment epithelium atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina pigment epithelium atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
seminal vesicle atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
sebaceous gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased susceptibility to induced muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
midbrain atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
epidermal atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney papillary atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
brain atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the brain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
exocrine pancreas atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hippocampus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hippocampus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
oviduct atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thymus medulla atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus medulla atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
facial muscle atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the facial muscle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Harderian gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Harderian gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
iris atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the iris atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
gastric gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the gastric gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skin atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skin atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased susceptibility to induced muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lymph node atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lymph node atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small intestinal villus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small intestinal villus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
forebrain atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the forebrain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
striatum atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the striatum atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
adrenal gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the adrenal gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pancreas atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle atrophy Gene Set From GO Biological Process Annotations 2025 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.
striated muscle atrophy Gene Set From GO Biological Process Annotations 2025 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.
Spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple system atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple system atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked spinal muscular atrophy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked spinal muscular atrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with lower extremity predominant from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Optic atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Optic atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Optic atrophy 3 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Optic atrophy 3 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with progressive myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Gyrate atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Gyrate atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Skin atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrophy of testis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gyrate atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dominant optic atrophy plus syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dominant optic atrophy plus syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Scapuloperoneal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scapuloperoneal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary choroidal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Olivopontocerebellar atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sveinsson chorioretinal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sveinsson chorioretinal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bosch-Boonstra-Schaaf optic atrophy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bosch-Boonstra-Schaaf optic atrophy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Partial optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pigmented paravenous chorioretinal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pigmented paravenous chorioretinal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset neurodegeneration with brain atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset neurodegeneration with brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked distal spinal muscular atrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinal muscular atrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinal muscular atrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant adult-onset proximal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant adult-onset proximal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset progressive encephalopathy with brain atrophy and thin corpus callosum Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset progressive encephalopathy with brain atrophy and thin corpus callosum in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrophy of prostate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy, Jokela type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy, Jokela type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy type 0 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy type 0 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gyrate atrophy of choroid and retina Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gyrate atrophy of choroid and retina phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive optic atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple system atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adult-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Scapuloperoneal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant optic atrophy classic form Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant optic atrophy classic form phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
OPA1-related optic atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the OPA1-related optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pigmented paravenous retinochoroidal atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pigmented paravenous retinochoroidal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hand muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hand muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy-progressive myoclonic epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-optic atrophy-Pelger-Huet anomaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-optic atrophy-Pelger-Huet anomaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bosch-Boonstra-Schaaf optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bosch-Boonstra-Schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Brain atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinocerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinocerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Limb-girdle muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microvillous atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Testicular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Testicular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset X-linked spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset X-linked spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral cortical atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral cortical atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Auditory neuropathy-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microcornea-myopic chorioretinal atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcornea-myopic chorioretinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leber optic atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dentatorubral-pallidoluysian atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dentatorubral-pallidoluysian atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrophy/Degeneration affecting the central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrophy/Degeneration affecting the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Posterior cortical atrophy and Alzheimer's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Posterior cortical atrophy and Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple system atrophy (pathologically confirmed) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple system atrophy (pathologically confirmed) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple system atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hippocampal atrophy rate Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hippocampal atrophy rate phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hippocampal atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hippocampal atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (geographic atrophy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (geographic atrophy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression to geographic atrophy form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to geographic atrophy form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe gastric atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe gastric atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Gastric atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastric atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
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.
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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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 Association 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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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 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.
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.
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 2015 genes participating in the regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal bipolar neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal bipolar neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal pigment epithelium development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal pigment epithelium development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal blood vessel morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal rod cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal rod cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal metabolic process Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal cell apoptotic process Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal cone cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cone cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of retinal cell programmed cell death Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of retinal cell programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of retinal ganglion cell axon guidance Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal rod cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the retinal rod cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
retinal dehydrogenase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
retinal isomerase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal isomerase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
all-trans retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the all-trans retinal binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
11-cis retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the 11-cis retinal binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
retinal binding Gene Set From GO Molecular Function Annotations 2015 genes performing the retinal binding molecular function from the curated GO Molecular Function Annotations 2015 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.
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 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 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 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.
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.
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 2014 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 2014 proteins participating in the Neural retinal development(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Eye-retinal bipolar neuron Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal bipolar neuron relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Eye-retinal blood vessel endothelial cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal blood vessel endothelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Eye-retinal ganglion cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal ganglion cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Eye-retinal pigment epithelial cell Gene Set From Tabula Sapiens Gene-Cell Associations genes with high or low expression in Eye-retinal pigment epithelial cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset.
Retinal Astrocytic Hamartoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Astrocytic Hamartoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Pigment Epithelial Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelial Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Toxicity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Toxicity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Vein Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Vein Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Telangiectasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Telangiectasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Venous Retinal Branch Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Venous Retinal Branch Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Vein Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Vein Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Necrosis Syndrome, Acute Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Necrosis Syndrome, Acute in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Retinal Degeneration (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Hamartoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Hamartoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Nonattachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Nonattachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Serous Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Serous Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Dysplasia And Retinal Aplasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Dysplasia And Retinal Aplasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhegmatogenous Retinal Detachment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhegmatogenous Retinal Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Angiomatous Proliferation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Angiomatous Proliferation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Drusen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Drusen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Retinal Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Retinal Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypertrophy Of Retinal Pigment Epithelium Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypertrophy Of Retinal Pigment Epithelium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Vasculitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Vasculitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Nonattachment, Nonsyndromic Congenital Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Nonattachment, Nonsyndromic Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculopathy, Retinal, With Cerebral Leukodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculopathy, Retinal, With Cerebral Leukodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystoid Macular Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystoid Macular Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Anomalies With Retinal And/Or Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Anomalies With Retinal And/Or Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Doyne Honeycomb Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Doyne Honeycomb Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Dystrophy With Early Macular Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Dystrophy With Early Macular Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Large Hyperpigmented Retinal Spots Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Large Hyperpigmented Retinal Spots in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Neovascularization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Retinal Neovascularization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glaucomatous Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Fibrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Fibrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Thrombosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Thrombosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Lattice Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Lattice Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rhegmatogenous Retinal Detachment, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rhegmatogenous Retinal Detachment, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Central Retinal Artery Occlusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Central Retinal Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Harmonizome 3.0

retinal atrophy Gene Set

Retinal atrophy Gene Set

muscular atrophy, spinal; spinal muscular atrophy Gene Set

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

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

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

Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set

geographic atrophy; macular degeneration; retinal drusen Gene Set

peripheral retinal atrophy Gene Set

retinal pigment epithelial atrophy Gene Set

retinal pigment epithelium atrophy Gene Set

Retinal Pigment Epithelium Atrophy Gene Set

Generalized Progressive Retinal Atrophy Gene Set

Progressive Retinal Atrophy Gene Set

Peripheral Retinal Atrophy Gene Set

Retinal Pigment Epithelial Atrophy Gene Set

Retinal pigment epithelial atrophy Gene Set

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

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

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

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

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

retinal artery occlusion; retinal vein occlusion Gene Set

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

Retinal detachment or retinal break Gene Set

Retinal detachment with retinal break Gene Set

Bosch-boonstra-schaaf optic atrophy syndrome Gene Set

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

Optic atrophy 7 Gene Set

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

Dominant hereditary optic atrophy Gene Set

Spinal muscular atrophy, type II Gene Set

Distal spinal muscular atrophy, X-linked 3 Gene Set

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

Spinal muscular atrophy Gene Set

X-linked myopathy with postural muscle atrophy Gene Set

Optic atrophy and cataract, autosomal dominant Gene Set

Optic Atrophy Type 1 Gene Set

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

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

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set

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

Congenital microvillous atrophy Gene Set

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

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

Distal spinal muscular atrophy, autosomal recessive 4 Gene Set

Sveinsson Chorioretinal Atrophy Gene Set

Optic Atrophy, Hereditary, Leber Gene Set

Spinal muscular atrophy, Jerash type Gene Set

Optic atrophy 1 and deafness Gene Set

Optic Atrophy 7 Gene Set

Optic Atrophy 4 Gene Set

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

Spinal muscular atrophy 4 Gene Set

Optic atrophy 5 Gene Set

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

Spinal muscular atrophy with respiratory distress 1 Gene Set

Atrophy Gene Set

Muscular Atrophy Gene Set

Myopathy, X-Linked, With Postural Muscle Atrophy Gene Set

Costeff optic atrophy syndrome Gene Set

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

Optic atrophy polyneuropathy deafness Gene Set

Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set

Chorioretinal atrophy, progressive bifocal Gene Set

Optic atrophy 6 Gene Set

Optic atrophy and cataract, autosomal dominant Gene Set

Gyrate Atrophy Gene Set

Optic Atrophy Gene Set

Pigmented Paravenous Chorioretinal Atrophy Gene Set

OPTIC ATROPHY 2 Gene Set

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

Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set

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

SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set

Optic Atrophy, Autosomal Dominant Gene Set

Muscular Atrophy, Spinal Gene Set

spinal muscular atrophy Gene Set