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Results for "skin atrophy": 1003 gene sets

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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.
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.
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.
dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
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.
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.
carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, light/dark/freckling skin] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 2, red hair/fair skin] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 2, blond hair/fair skin] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, blond hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 5, dark/fair skin] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 4, fair/dark skin] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 4, fair/dark skin] phenotype from the curated OMIM Gene-Disease Associations dataset.
Acute Bacterial Skin And Skin Structure Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Bacterial Skin And Skin Structure Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complicated Skin And Skin Structure Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complicated Skin And Skin Structure Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Skin Gene Set From BioGPS Human Cell Type and Tissue Gene Expression Profiles genes with high or low expression in Skin relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
Skin/hair/eye pigmentation, variation in, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Inflammatory skin and bowel disease, neonatal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Inflammatory skin and bowel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stiff skin syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Stiff skin syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dominant dystrophic epidermolysis bullosa with absence of skin Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant dystrophic epidermolysis bullosa with absence of skin phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin fragility woolly hair syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin fragility woolly hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypotrichosis and recurrent skin vesicles Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypotrichosis and recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ectodermal dysplasia skin fragility syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peeling skin syndrome, acral type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peeling skin syndrome, acral type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Tight skin contracture syndrome, lethal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tight skin contracture syndrome, lethal from the curated CTD Gene-Disease Associations dataset.
Skin Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skin Diseases from the curated CTD Gene-Disease Associations dataset.
Skin Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skin Abnormalities from the curated CTD Gene-Disease Associations dataset.
Wrinkly skin syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wrinkly skin syndrome from the curated CTD Gene-Disease Associations dataset.
Hypotrichosis And Recurrent Skin Vesicles Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypotrichosis And Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.
Skin Diseases, Vascular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skin Diseases, Vascular from the curated CTD Gene-Disease Associations dataset.
Skin Ulcer Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skin Ulcer from the curated CTD Gene-Disease Associations dataset.
PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset.
Skin Fragility-Woolly Hair Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skin Fragility-Woolly Hair Syndrome from the curated CTD Gene-Disease Associations dataset.
Ectodermal dysplasia/ skin fragility syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia/ skin fragility syndrome from the curated CTD Gene-Disease Associations dataset.
Peeling Skin Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peeling Skin Syndrome from the curated CTD Gene-Disease Associations dataset.
Stiff Skin Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stiff Skin Syndrome from the curated CTD Gene-Disease Associations dataset.
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.
Skin Neoplasms Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Skin Neoplasms from the curated CTD Gene-Disease Associations dataset.
Peeling skin syndrome, acral type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peeling skin syndrome, acral type from the curated CTD Gene-Disease Associations dataset.
Skin Pigmentation Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Skin Pigmentation in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
skin disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease skin disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
vascular skin disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease vascular skin disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
skin benign neoplasm Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease skin benign neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
vesiculobullous skin disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease vesiculobullous skin disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
skin cancer Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease skin cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
skin disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease skin disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
vascular skin disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease vascular skin disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
skin melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
verruciform xanthoma of skin Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease verruciform xanthoma of skin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin squamous cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin sarcoidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin sarcoidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
malignant skin fibrous histiocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant skin fibrous histiocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sarcomatoid squamous cell skin carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sarcomatoid squamous cell skin carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autoimmune disease of skin and connective tissue Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autoimmune disease of skin and connective tissue in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bullous skin disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bullous skin disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin lipoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin carcinoma in situ Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin carcinoma in situ in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vesiculobullous skin disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vesiculobullous skin disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
eccrine mixed tumor of skin Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eccrine mixed tumor of skin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin papilloma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin papilloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin pilomatrix carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin pilomatrix carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vascular skin disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vascular skin disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin tag Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin tag in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic ulcer of skin Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic ulcer of skin in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin hemangioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin hemangioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
H3K4me3_fibroblast of skin of abdomen_hg19_1 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of skin of abdomen_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
H3K4me3_fibroblast of skin of abdomen_hg19_2 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of skin of abdomen_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
CTCF_fibroblast of skin of abdomen_hg19_2 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of skin of abdomen_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
CTCF_fibroblast of skin of abdomen_hg19_1 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of skin of abdomen_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma, t-cell, cutaneous; lymphoma, t-cell, peripheral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin cancer, nonmelanoma Gene Set From GAD Gene-Disease Associations genes associated with the disease skin cancer, nonmelanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; nevus; skin neoplasms; sunburn Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; nevus; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
precancerous conditions; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; disease susceptibility; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; disease susceptibility; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases; sarcoidosis; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases; sarcoidosis; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; nevus; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erythema; psoriasis; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease erythema; psoriasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma, amelanotic; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma, amelanotic; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lymphoma, t-cell, cutaneous; parapsoriasis; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease lymphoma, t-cell, cutaneous; parapsoriasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin color Gene Set From GAD Gene-Disease Associations genes associated with the disease skin color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung cancer; skin cancer, non-melanoma Gene Set From GAD Gene-Disease Associations genes associated with the disease lung cancer; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease skin cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; skin cancer, non-melanoma Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin cancer; squamous cell carcinoma; carcinoma, basal cell Gene Set From GAD Gene-Disease Associations genes associated with the disease skin cancer; squamous cell carcinoma; carcinoma, basal cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
psoriasis; skin diseases, genetic Gene Set From GAD Gene-Disease Associations genes associated with the disease psoriasis; skin diseases, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
papillomavirus infections; skin neoplasms; sunburn; tumor virus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease papillomavirus infections; skin neoplasms; sunburn; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; neoplasm invasiveness; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasm invasiveness; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
erythema; rare diseases; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease erythema; rare diseases; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin condition Gene Set From GAD Gene-Disease Associations genes associated with the disease skin condition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms, basal cell; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms, basal cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin cancer, non-melanoma Gene Set From GAD Gene-Disease Associations genes associated with the disease skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; skin basal cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; skin basal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin diseases; sunburn Gene Set From GAD Gene-Disease Associations genes associated with the disease skin diseases; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage; neoplasms; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage; neoplasms; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; skin neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin carcinomas Gene Set From GAD Gene-Disease Associations genes associated with the disease skin carcinomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cell transformation, neoplastic; epidermodysplasia verruciformis; papillomavirus infections; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; epidermodysplasia verruciformis; papillomavirus infections; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cell transformation, neoplastic; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease lupus erythematosus, cutaneous; lupus erythematosus, discoid; photosensitivity disorders; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set From GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
edema; hypertension; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease edema; hypertension; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
keratosis; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease keratosis; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; papillomavirus infections; skin neoplasms; squamous cell carcinoma; tumor virus infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; skin diseases, vesiculobullous Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; skin diseases, vesiculobullous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; skin neoplasms; sunburn Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arsenic poisoning; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease arsenic poisoning; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; neoplasms, multiple primary; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
keratosis; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease keratosis; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin cancer; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease skin cancer; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin sensitivity to sun Gene Set From GAD Gene-Disease Associations genes associated with the disease skin sensitivity to sun in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin neoplasms; sunburn Gene Set From GAD Gene-Disease Associations genes associated with the disease skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
facial neoplasms; horse diseases; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease facial neoplasms; horse diseases; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypersensitivity; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hypersensitivity; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin lesion Gene Set From GAD Gene-Disease Associations genes associated with the disease skin lesion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autoimmune diseases; skin diseases, genetic; vitiligo Gene Set From GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; skin diseases, genetic; vitiligo in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease connective tissue diseases; fetal diseases; inflammation; musculoskeletal diseases; pregnancy complications, hematologic; premature birth; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis; sarcoidosis; skin diseases; syndrome; uveitis; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperpigmentation; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperpigmentation; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease skin squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; neoplasm metastasis; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasm metastasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
breast neoplasms; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease breast neoplasms; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
scleroderma, systemic; skin ulcer; systemic scleroderma Gene Set From GAD Gene-Disease Associations genes associated with the disease scleroderma, systemic; skin ulcer; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin pigmentation Gene Set From GAD Gene-Disease Associations genes associated with the disease skin pigmentation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
scleroderma, systemic; skin ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease scleroderma, systemic; skin ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dysplastic nevus syndrome; melanoma; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease dysplastic nevus syndrome; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma skin cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma skin cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cocarcinogenesis; skin neoplasms; sunburn Gene Set From GAD Gene-Disease Associations genes associated with the disease cocarcinogenesis; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
microsatellite instability; nevus, pigmented; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease microsatellite instability; nevus, pigmented; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; skin diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cutaneous melanoma which is largely independent of skin type and hair color Gene Set From GAD Gene-Disease Associations genes associated with the disease cutaneous melanoma which is largely independent of skin type and hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
melanoma; nevus; precancerous conditions; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease melanoma; nevus; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma Gene Set From GAD Gene-Disease Associations genes associated with the disease hypertension, pulmonary; raynaud disease; scleroderma, systemic; skin ulcer; systemic scleroderma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mycobacterium infections, atypical; skin ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease mycobacterium infections, atypical; skin ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
carcinoma, squamous cell; cell transformation, neoplastic; skin neoplasms; squamous cell carcinoma Gene Set From GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; cell transformation, neoplastic; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
severe photoaging of facial skin Gene Set From GAD Gene-Disease Associations genes associated with the disease severe photoaging of facial skin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
skin Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term skin in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Get-1_Deficiency_GDS2629_161_mouse_embryonic skin Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Get-1_Deficiency_GDS2629_161_mouse_embryonic skin gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
regulation of water loss via skin Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of water loss via skin biological process from the curated GO Biological Process Annotations 2015 dataset.
establishment of skin barrier Gene Set From GO Biological Process Annotations 2015 genes participating in the establishment of skin barrier biological process from the curated GO Biological Process Annotations 2015 dataset.
skin development Gene Set From GO Biological Process Annotations 2015 genes participating in the skin development biological process from the curated GO Biological Process Annotations 2015 dataset.
skin epidermis development Gene Set From GO Biological Process Annotations 2015 genes participating in the skin epidermis development biological process from the curated GO Biological Process Annotations 2015 dataset.
skin morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the skin morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
skin Gene Set From GTEx Tissue Gene Expression Profiles genes with high or low expression in skin relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.
Skin sensitivity to sun Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Skin sensitivity to sun phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Skin pigmentation Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Skin pigmentation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Non-melanoma skin cancer Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Non-melanoma skin cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
skin melanoma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease skin melanoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
skin cancer Gene Set From GWASdb SNP-Disease Associations genes associated with the disease skin cancer in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
skin disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease skin disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
bullous skin disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease bullous skin disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
skin carcinoma Gene Set From GWASdb SNP-Disease Associations genes associated with the disease skin carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
inflammatory abnormality of the skin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
neoplasm of the skin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the neoplasm of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
localized skin lesion Gene Set From GWASdb SNP-Phenotype Associations genes associated with the localized skin lesion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of skin adnexa Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of skin morphology Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the skin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
vascular skin abnormality Gene Set From GWASdb SNP-Phenotype Associations genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
atypical scarring of skin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the atypical scarring of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
skin rash Gene Set From GWASdb SNP-Phenotype Associations genes associated with the skin rash phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of skin physiology Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
generalized abnormality of skin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of skin pigmentation Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
skin Gene Set From HPA Tissue Gene Expression Profiles genes with high or low expression in skin relative to other tissues from the HPA Tissue Gene Expression Profiles dataset.
skin Gene Set From HPA Tissue Protein Expression Profiles proteins with high or low expression in skin relative to other tissues from the HPA Tissue Protein Expression Profiles dataset.
dry skin Gene Set From HPO Gene-Disease Associations genes associated with the dry skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thin skin Gene Set From HPO Gene-Disease Associations genes associated with the thin skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reticulated skin pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the reticulated skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
telangiectases in sun-exposed and nonexposed skin Gene Set From HPO Gene-Disease Associations genes associated with the telangiectases in sun-exposed and nonexposed skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the skin Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized abnormality of skin Gene Set From HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypopigmentation of the skin Gene Set From HPO Gene-Disease Associations genes associated with the hypopigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal delayed hypersensitivity skin test Gene Set From HPO Gene-Disease Associations genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
inflammatory abnormality of the skin Gene Set From HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin ulcer Gene Set From HPO Gene-Disease Associations genes associated with the skin ulcer phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fine, reticulate skin pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the fine, reticulate skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
punctate vasculitis skin lesions Gene Set From HPO Gene-Disease Associations genes associated with the punctate vasculitis skin lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
profuse pigmented skin lesions Gene Set From HPO Gene-Disease Associations genes associated with the profuse pigmented skin lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital localized absence of skin Gene Set From HPO Gene-Disease Associations genes associated with the congenital localized absence of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
excessive wrinkling of palmar skin Gene Set From HPO Gene-Disease Associations genes associated with the excessive wrinkling of palmar skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the skin Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of skin adnexa Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of skin adnexa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
postauricular skin tag Gene Set From HPO Gene-Disease Associations genes associated with the postauricular skin tag phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
blotching pigmentation of the skin Gene Set From HPO Gene-Disease Associations genes associated with the blotching pigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the plantar skin of foot Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the plantar skin of foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin erosion Gene Set From HPO Gene-Disease Associations genes associated with the skin erosion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin tags Gene Set From HPO Gene-Disease Associations genes associated with the skin tags phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vascular skin abnormality Gene Set From HPO Gene-Disease Associations genes associated with the vascular skin abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal elasticity of skin Gene Set From HPO Gene-Disease Associations genes associated with the abnormal elasticity of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
localized skin lesion Gene Set From HPO Gene-Disease Associations genes associated with the localized skin lesion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypopigmented skin patches on arms Gene Set From HPO Gene-Disease Associations genes associated with the hypopigmented skin patches on arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stiff skin Gene Set From HPO Gene-Disease Associations genes associated with the stiff skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin dimple over apex of long bone angulation Gene Set From HPO Gene-Disease Associations genes associated with the skin dimple over apex of long bone angulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
periauricular skin pits Gene Set From HPO Gene-Disease Associations genes associated with the periauricular skin pits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
redundant skin Gene Set From HPO Gene-Disease Associations genes associated with the redundant skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atypical scarring of skin Gene Set From HPO Gene-Disease Associations genes associated with the atypical scarring of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
desquamation of skin soon after birth Gene Set From HPO Gene-Disease Associations genes associated with the desquamation of skin soon after birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin nodule Gene Set From HPO Gene-Disease Associations genes associated with the skin nodule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
excessive wrinkled skin Gene Set From HPO Gene-Disease Associations genes associated with the excessive wrinkled skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
midline skin dimples over anterior/posterior fontanelles Gene Set From HPO Gene-Disease Associations genes associated with the midline skin dimples over anterior/posterior fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neonatal wrinkled skin of hands and feet Gene Set From HPO Gene-Disease Associations genes associated with the neonatal wrinkled skin of hands and feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vasculitis in the skin Gene Set From HPO Gene-Disease Associations genes associated with the vasculitis in the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
redundant skin on fingers Gene Set From HPO Gene-Disease Associations genes associated with the redundant skin on fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hyperextensible skin Gene Set From HPO Gene-Disease Associations genes associated with the hyperextensible skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
redundant neck skin Gene Set From HPO Gene-Disease Associations genes associated with the redundant neck skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
preauricular skin tag Gene Set From HPO Gene-Disease Associations genes associated with the preauricular skin tag phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
squamous cell carcinoma of the skin Gene Set From HPO Gene-Disease Associations genes associated with the squamous cell carcinoma of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of skin morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of skin morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thickened nuchal skin fold Gene Set From HPO Gene-Disease Associations genes associated with the thickened nuchal skin fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
premature skin wrinkling Gene Set From HPO Gene-Disease Associations genes associated with the premature skin wrinkling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal blistering of the skin Gene Set From HPO Gene-Disease Associations genes associated with the abnormal blistering of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmentation anomalies of sun-exposed skin Gene Set From HPO Gene-Disease Associations genes associated with the pigmentation anomalies of sun-exposed skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hyperpigmentation of the skin Gene Set From HPO Gene-Disease Associations genes associated with the hyperpigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
neoplasm of the skin Gene Set From HPO Gene-Disease Associations genes associated with the neoplasm of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
preauricular skin furrow Gene Set From HPO Gene-Disease Associations genes associated with the preauricular skin furrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
soft skin Gene Set From HPO Gene-Disease Associations genes associated with the soft skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypertrophy of skin of soles Gene Set From HPO Gene-Disease Associations genes associated with the hypertrophy of skin of soles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypopigmented skin patches Gene Set From HPO Gene-Disease Associations genes associated with the hypopigmented skin patches phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
warfarin-induced skin necrosis Gene Set From HPO Gene-Disease Associations genes associated with the warfarin-induced skin necrosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin vesicle Gene Set From HPO Gene-Disease Associations genes associated with the skin vesicle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of skin pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent skin infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin rash Gene Set From HPO Gene-Disease Associations genes associated with the skin rash phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
yellow subcutaneous tissue covered by thin, scaly skin Gene Set From HPO Gene-Disease Associations genes associated with the yellow subcutaneous tissue covered by thin, scaly skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lack of skin elasticity Gene Set From HPO Gene-Disease Associations genes associated with the lack of skin elasticity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fragile skin Gene Set From HPO Gene-Disease Associations genes associated with the fragile skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin dimples Gene Set From HPO Gene-Disease Associations genes associated with the skin dimples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
depigmentation/hyperpigmentation of skin Gene Set From HPO Gene-Disease Associations genes associated with the depigmentation/hyperpigmentation of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of skin physiology Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of skin physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mixed hypo- and hyperpigmentation of the skin Gene Set From HPO Gene-Disease Associations genes associated with the mixed hypo- and hyperpigmentation of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
soft, doughy skin Gene Set From HPO Gene-Disease Associations genes associated with the soft, doughy skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
regional abnormality of skin Gene Set From HPO Gene-Disease Associations genes associated with the regional abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent bacterial skin infections Gene Set From HPO Gene-Disease Associations genes associated with the recurrent bacterial skin infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin fragility with non-scarring blistering Gene Set From HPO Gene-Disease Associations genes associated with the skin fragility with non-scarring blistering phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
teleangiectasia of the skin Gene Set From HPO Gene-Disease Associations genes associated with the teleangiectasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormally lax or hyperextensible skin Gene Set From HPO Gene-Disease Associations genes associated with the abnormally lax or hyperextensible skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
asymmetric, linear skin defects Gene Set From HPO Gene-Disease Associations genes associated with the asymmetric, linear skin defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thickened skin Gene Set From HPO Gene-Disease Associations genes associated with the thickened skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent skin pigmentation Gene Set From HPO Gene-Disease Associations genes associated with the absent skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skin pit Gene Set From HPO Gene-Disease Associations genes associated with the skin pit phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Skin Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Abnormalities Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Abnormalities phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Ulcer Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Ulcer phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Diseases, Genetic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases, Genetic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Diseases, Viral Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases, Viral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Galvanic Skin Response Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Galvanic Skin Response phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Diseases, Parasitic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases, Parasitic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Diseases, Vesiculobullous Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases, Vesiculobullous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Diseases, Vascular Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases, Vascular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Diseases, Bacterial Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases, Bacterial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Staphylococcal Skin Infections Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Staphylococcal Skin Infections phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Diseases, Metabolic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Diseases, Metabolic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skin Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Skin-specific protein 32 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Skin-specific protein 32 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
dry skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dry skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin condition Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin condition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
reddish skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the reddish skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skin turgor Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skin turgor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin exfoliation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin exfoliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skin tensile strength Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skin tensile strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
scaly skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the scaly skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
blotchy skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the blotchy skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin lesions Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin lesions phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
wrinkled skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the wrinkled skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
calcified skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the calcified skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin sebaceous gland morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin sebaceous gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
tight skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the tight skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed skin barrier formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed skin barrier formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
flaky skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the flaky skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin adnexa morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin adnexa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
shiny skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the shiny skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
loose skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the loose skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spontaneous skin ulceration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spontaneous skin ulceration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased sensitivity to skin irradiation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased sensitivity to skin irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin adnexa physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin adnexa physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
impaired skin barrier function Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired skin barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
translucent skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the translucent skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin coloration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin coloration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased skin squamous cell carcinoma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased skin squamous cell carcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sensitivity to skin irradiation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to skin irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skin pigmentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skin pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin edema Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin edema phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin pigmentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin photosensitivity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin photosensitivity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased skin tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased skin tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
oily skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the oily skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin tensile strength Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin tensile strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin detachment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin detachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin turgor Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin turgor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thick skin Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thick skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin hyperplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin appearance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin appearance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent skin pigmentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent skin pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased skin papilloma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased skin papilloma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin physiology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skin fibrosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skin fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
[skin/hair/eye pigmentation 6, blond/brown hair] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 6, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.
[tuberculin skin test reactivity, absence of] Gene Set From OMIM Gene-Disease Associations genes associated with the [tuberculin skin test reactivity, absence of] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 3, blue/green eyes] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation, variation in, 8] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 8] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 9, dark/light hair] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, dark/light hair] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 10, blond/brown hair] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 10, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 6, blue/green eyes] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 6, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 5, black/nonblack hair] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, black/nonblack hair] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 1, blue/nonblue eyes] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 1, blue/nonblue eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.
stiff skin syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the stiff skin syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 7, blond/brown hair] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 7, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.
?hypotrichosis and recurrent skin vesicles Gene Set From OMIM Gene-Disease Associations genes associated with the ?hypotrichosis and recurrent skin vesicles phenotype from the curated OMIM Gene-Disease Associations dataset.
[tuberculin skin test reactivity qtl] Gene Set From OMIM Gene-Disease Associations genes associated with the [tuberculin skin test reactivity qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
?inflammatory skin and bowel disease, neonatal, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the ?inflammatory skin and bowel disease, neonatal, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] phenotype from the curated OMIM Gene-Disease Associations dataset.
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal Gene Set From OMIM Gene-Disease Associations genes associated with the palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal phenotype from the curated OMIM Gene-Disease Associations dataset.
ectodermal dysplasia/skin fragility syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia/skin fragility syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 5, dark/light eyes] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/light eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.
{uv-induced skin damage} Gene Set From OMIM Gene-Disease Associations genes associated with the {uv-induced skin damage} phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 9, brown/nonbrown eyes] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, brown/nonbrown eyes] phenotype from the curated OMIM Gene-Disease Associations dataset.
wrinkly skin syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the wrinkly skin syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation 1, blond/brown hair] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 1, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset.
peeling skin syndrome 1 Gene Set From OMIM Gene-Disease Associations genes associated with the peeling skin syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
peeling skin syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the peeling skin syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
skin fragility-woolly hair syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the skin fragility-woolly hair syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
skin Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term skin in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EB-A44Q-06A-11R-A266-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EB-A44Q-06A-11R-A266-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EB-A42Y-01A-12R-A24X-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EB-A42Y-01A-12R-A24X-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EE-A2MK-06A-11R-A18S-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EE-A2MK-06A-11R-A18S-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EE-A2M8-06A-12R-A18S-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EE-A2M8-06A-12R-A18S-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-ER-A2ND-06A-11R-A18T-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-ER-A2ND-06A-11R-A18T-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-D3-A5GR-06A-11R-A27Q-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-D3-A5GR-06A-11R-A27Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EB-A5SH-06A-11R-A311-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EB-A5SH-06A-11R-A311-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-D3-A1Q6-06A-11R-A18T-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-D3-A1Q6-06A-11R-A18T-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-ER-A19Q-06A-11R-A18U-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-ER-A19Q-06A-11R-A18U-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-FS-A1ZW-06A-12R-A18T-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-FS-A1ZW-06A-12R-A18T-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-FS-A1ZH-06A-11R-A18T-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-FS-A1ZH-06A-11R-A18T-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EB-A51B-01A-11R-A27Q-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EB-A51B-01A-11R-A27Q-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EB-A42Z-01A-12R-A24X-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EB-A42Z-01A-12R-A24X-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-ER-A19M-06A-61R-A239-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-ER-A19M-06A-61R-A239-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EB-A3XD-01A-22R-A239-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EB-A3XD-01A-22R-A239-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-D3-A2JA-06A-11R-A18T-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-D3-A2JA-06A-11R-A18T-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-BF-A1Q0-01A-21R-A18S-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-BF-A1Q0-01A-21R-A18S-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-DA-A3F2-06A-11R-A20F-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-DA-A3F2-06A-11R-A20F-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-D3-A3C7-06A-11R-A18U-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-D3-A3C7-06A-11R-A18U-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-BF-A1PV-01A-11R-A18U-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-BF-A1PV-01A-11R-A18U-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-EB-A5VU-01A-21R-A32P-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-EB-A5VU-01A-21R-A32P-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-D3-A1Q5-06A-11R-A18T-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-D3-A1Q5-06A-11R-A18T-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-GN-A263-01A-11R-A18T-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-GN-A263-01A-11R-A18T-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.
Skin Cutaneous Melanoma_SKCM_TCGA-ER-A19J-06A-11R-A18S-07 Gene Set From TCGA Signatures of Differentially Expressed Genes for Tumors genes with high or low expression in Skin Cutaneous Melanoma_SKCM_TCGA-ER-A19J-06A-11R-A18S-07 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Harmonizome 3.0

skin atrophy Gene Set

skin atrophy Gene Set

Skin atrophy Gene Set

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

diffuse skin atrophy Gene Set

Diffuse Skin Atrophy Gene Set

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms Gene Set

carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms Gene Set

carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms Gene Set

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene Set

[skin/hair/eye pigmentation 2, red hair/fair skin] Gene Set

[skin/hair/eye pigmentation 2, blond hair/fair skin] Gene Set

[skin/hair/eye pigmentation 5, dark/fair skin] Gene Set

[skin/hair/eye pigmentation 4, fair/dark skin] Gene Set

Acute Bacterial Skin And Skin Structure Infection Gene Set

Complicated Skin And Skin Structure Infection 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