optic atrophy 3 with cataract

Filters:

Results for "optic atrophy 3 with cataract": 16 genes, 1001 gene sets

Name
OPA6 Gene optic atrophy 6 (autosomal recessive)
OPA4 Gene optic atrophy 4 (autosomal dominant)
OPA5 Gene optic atrophy 5 (autosomal dominant)
OPA2 Gene optic atrophy 2 (obscure)
OPA1 Gene optic atrophy 1 (autosomal dominant) The protein encoded by this gene is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. The encoded protein localizes to the inner mitochondrial membrane and helps regulate mitochondrial stability and energy output. This protein also sequesters cytochrome c. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. [provided by RefSeq, Aug 2017]
OPA3 Gene optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
SPOAN Gene spastic paraplegia, optic* atrophy, and neuropathy*
LOAS Gene Leber optic* atrophy, susceptibility to*
CODA Gene Cavitary optic* disc anomalies*
GUST Gene Gustavson mental retardation syndrome (with microcephaly, optic
PBCRA1 Gene progressive bifocal chorioretinal atrophy* 1*
CLAM Gene cerebellar atrophy* with progressive microcephaly*
SMAR Gene Spinal muscular atrophy, chronic distal, autosomal recessive
SMAL Gene spinal muscular atrophy, congenital nonprogressive, of lower limbs
SCA18 Gene spinocerebellar ataxia 18 (sensory with* neurogenic muscular atrophy)*
SMAJ Gene Spinal muscular atrophy, Jokela type
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.
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic 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 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 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.
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.
disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Bosch-boonstra-schaaf optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dominant hereditary optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic Atrophy Type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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.
Optic Atrophy, Hereditary, Leber Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 1 and deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 5 from the curated CTD Gene-Disease Associations dataset.
Costeff optic atrophy syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset.
Optic atrophy polyneuropathy deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic 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.
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.
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.
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.
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.
optic disc atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease optic disc atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, hereditary, leber; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy and moderate deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy and moderate deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic 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.
leber optic atrophy Gene Set From HPO Gene-Disease Associations genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic atrophy from cranial nerve compression Gene Set From HPO Gene-Disease Associations genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Optic Atrophy, Hereditary, Leber Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic 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.
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.
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.
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.
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.
short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.
?neurodegeneration with optic atrophy, childhood onset Gene Set From OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy plus syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
{leber optic atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Optic 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.
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.
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.
Dominant Hereditary Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Hereditary Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Foveal hypoplasia and presenile cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, posterior polar, 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, posterior polar, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Zonular pulverulent cataract 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Zonular pulverulent cataract 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 15, multiple types Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 15, multiple types phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal dominant, multiple types, with microcornea Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, nuclear total Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, nuclear total phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperferritinemia cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperferritinemia cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Absent corpus callosum cataract immunodeficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Absent corpus callosum cataract immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal recessive congenital 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, zonular Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, zonular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract and cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, microphthalmia and nystagmus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, membranous Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, membranous phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, juvenile, with microcornea and glucosuria Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital nuclear, autosomal recessive 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Posterior polar cataract type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Posterior polar cataract type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Adult i Blood Group with or without Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 23 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, congenital Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cataract congenital Volkmann type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.
Cataract, Nuclear Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Nuclear Progressive from the curated CTD Gene-Disease Associations dataset.
Cataract, Central Saccular, With Sutural Opacities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Central Saccular, With Sutural Opacities from the curated CTD Gene-Disease Associations dataset.
Cataract, posterior polar, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, posterior polar, 4 from the curated CTD Gene-Disease Associations dataset.
Cataract, posterior polar, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, posterior polar, 3 from the curated CTD Gene-Disease Associations dataset.
Cerulean cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerulean cataract from the curated CTD Gene-Disease Associations dataset.
Cataract, Zonular Pulverulent 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Zonular Pulverulent 3 from the curated CTD Gene-Disease Associations dataset.
Cataract, Zonular Pulverulent 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Zonular Pulverulent 1 from the curated CTD Gene-Disease Associations dataset.
Cataract, Juvenile, With Microcornea And Glucosuria Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.
Absent corpus callosum cataract immunodeficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Absent corpus callosum cataract immunodeficiency from the curated CTD Gene-Disease Associations dataset.
CATARACT 32, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 32, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Zonular, with Sutural Opacities Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Zonular, with Sutural Opacities from the curated CTD Gene-Disease Associations dataset.
CATARACT 6, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 6, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Cataract and cardiomyopathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset.
Cataract, Age-Related Cortical, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Age-Related Cortical, 1 from the curated CTD Gene-Disease Associations dataset.
Cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.
Anterior polar cataract 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Anterior polar cataract 2 from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Recessive Congenital 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Recessive Congenital 3 from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Recessive, Early-Onset, Pulverulent Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Recessive, Early-Onset, Pulverulent from the curated CTD Gene-Disease Associations dataset.
Cataract, Autosomal Dominant, Multiple Types 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Autosomal Dominant, Multiple Types 1 from the curated CTD Gene-Disease Associations dataset.
Cataract microcornea syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract microcornea syndrome from the curated CTD Gene-Disease Associations dataset.
Cataract, Cortical, Juvenile-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Cortical, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.
Cataract, zonular Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, zonular from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 1 from the curated CTD Gene-Disease Associations dataset.
CATARACT 3, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 3, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Cataract, congenital, with microcornea or slight microphthalmia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, congenital, with microcornea or slight microphthalmia from the curated CTD Gene-Disease Associations dataset.
Cataract, Pulverulent, Juvenile-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Pulverulent, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Cataract 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 2 from the curated CTD Gene-Disease Associations dataset.
Microphthalmia, Isolated, with Cataract 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 1 from the curated CTD Gene-Disease Associations dataset.
CATARACT 4, MULTIPLE TYPES Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 4, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.
Cataract, Coppock-Like Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Coppock-Like from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.
CATARACT, CONGENITAL OR JUVENILE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT, CONGENITAL OR JUVENILE from the curated CTD Gene-Disease Associations dataset.
Cataract, Congenital Nuclear, Autosomal Recessive 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.
CATARACT 23 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CATARACT 23 from the curated CTD Gene-Disease Associations dataset.
cataract Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cataract from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
senile cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
morgagni cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease morgagni cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mature cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
immature cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease immature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
posterior polar cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior polar cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diabetic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diabetic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital nuclear cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease congenital nuclear cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; exfoliation syndrome; glaucoma, open-angle Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; exfoliation syndrome; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
zonular pulverulent cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease zonular pulverulent cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; exfoliation syndrome; glaucoma; glaucoma, open-angle Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; exfoliation syndrome; glaucoma; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant coral-like cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant coral-like cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract, presenile Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract, presenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cataract in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cataract Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cataract in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
cataract Gene Set From GWASdb SNP-Phenotype Associations genes associated with the cataract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
anterior polar cataract Gene Set From HPO Gene-Disease Associations genes associated with the anterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
juvenile cataract Gene Set From HPO Gene-Disease Associations genes associated with the juvenile cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cataract Gene Set From HPO Gene-Disease Associations genes associated with the progressive cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pulverulent cataract Gene Set From HPO Gene-Disease Associations genes associated with the pulverulent cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior subcapsular cataract Gene Set From HPO Gene-Disease Associations genes associated with the posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital nuclear cataract Gene Set From HPO Gene-Disease Associations genes associated with the congenital nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sutural cataract Gene Set From HPO Gene-Disease Associations genes associated with the sutural cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
iridescent posterior subcapsular cataract Gene Set From HPO Gene-Disease Associations genes associated with the iridescent posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior cortical cataract Gene Set From HPO Gene-Disease Associations genes associated with the posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
polar cataract Gene Set From HPO Gene-Disease Associations genes associated with the polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cortical cataract Gene Set From HPO Gene-Disease Associations genes associated with the cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior polar cataract Gene Set From HPO Gene-Disease Associations genes associated with the posterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
total cataract Gene Set From HPO Gene-Disease Associations genes associated with the total cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerulean cataract Gene Set From HPO Gene-Disease Associations genes associated with the cerulean cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
punctate cataract Gene Set From HPO Gene-Disease Associations genes associated with the punctate cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
posterior y-sutural cataract Gene Set From HPO Gene-Disease Associations genes associated with the posterior y-sutural cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
zonular cataract Gene Set From HPO Gene-Disease Associations genes associated with the zonular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
juvenile cortical cataract Gene Set From HPO Gene-Disease Associations genes associated with the juvenile cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dense posterior cortical cataract Gene Set From HPO Gene-Disease Associations genes associated with the dense posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital cataract Gene Set From HPO Gene-Disease Associations genes associated with the congenital cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cortical pulverulent cataract Gene Set From HPO Gene-Disease Associations genes associated with the cortical pulverulent cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
membranous cataract Gene Set From HPO Gene-Disease Associations genes associated with the membranous cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse nuclear cataract Gene Set From HPO Gene-Disease Associations genes associated with the diffuse nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcapsular cataract Gene Set From HPO Gene-Disease Associations genes associated with the subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nuclear cataract Gene Set From HPO Gene-Disease Associations genes associated with the nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cataract Gene Set From HPO Gene-Disease Associations genes associated with the cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lamellar cataract Gene Set From HPO Gene-Disease Associations genes associated with the lamellar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cataract Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cataract phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
cataract 5, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 5, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 36 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 36 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract, juvenile, with microcornea and glucosuria Gene Set From OMIM Gene-Disease Associations genes associated with the cataract, juvenile, with microcornea and glucosuria phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 40, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 40, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set From OMIM Gene-Disease Associations genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 9, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 9, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract with late-onset corneal dystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopia, high, with cataract and vitreoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 30, pulverulent Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 30, pulverulent phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 22, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 22, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, cataract, retinitis pigmentosa, and sperm abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, cataract, retinitis pigmentosa, and sperm abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 3, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 3, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataract 41 Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataract 41 phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataract 42 Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataract 42 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 1, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 1, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 29, coralliform Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 29, coralliform phenotype from the curated OMIM Gene-Disease Associations dataset.
{cataract 28, age-related cortical, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {cataract 28, age-related cortical, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 20, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 20, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 33 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 33 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 14, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 14, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 19 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 19 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 37, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 12, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 12, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 39, multiple types, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperferritinemia-cataract syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the hyperferritinemia-cataract syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set From OMIM Gene-Disease Associations genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 34, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 34, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 11, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 11, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract, pulverulent or cerulean, with or without microcornea Gene Set From OMIM Gene-Disease Associations genes associated with the cataract, pulverulent or cerulean, with or without microcornea phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 6, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 6, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 2, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 2, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 16, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 16, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 15, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 15, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
adult i phenotype without cataract Gene Set From OMIM Gene-Disease Associations genes associated with the adult i phenotype without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 11, syndromic Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 11, syndromic phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 18, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 18, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataract, congenital Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataract, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 17, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 17, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 25 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 23 Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 23 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 27, nuclear progressive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 27, nuclear progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 4, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 4, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 31, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 31, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 10, multiple types Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 10, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.
anterior segment anomalies with or without cataract Gene Set From OMIM Gene-Disease Associations genes associated with the anterior segment anomalies with or without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 38, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 38, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia with cataract 2 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia with cataract 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
microphthalmia with cataract 1 Gene Set From OMIM Gene-Disease Associations genes associated with the microphthalmia with cataract 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 13 with adult i phenotype Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 13 with adult i phenotype phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 35, congenital nuclear Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 35, congenital nuclear phenotype from the curated OMIM Gene-Disease Associations dataset.
Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcapsular Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Subcapsular Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
After-Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease After-Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cortical Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nuclear Non-Senile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nuclear Non-Senile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonnuclear Polymorphic Congenital Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonnuclear Polymorphic Congenital Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Subcapsular Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Other Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Other Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Total Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Total Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Age-Related Cortical Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Induced Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Induced Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Age-Related Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Lamellar Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Lamellar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unilateral Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unilateral Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Presenile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Presenile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cortical, Lamellar, Or Zonular Nonsenile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cortical, Lamellar, Or Zonular Nonsenile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Embryonal Nuclear Cataract (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Embryonal Nuclear Cataract (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nuclear Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nuclear Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sutural Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sutural Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polar Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Morgagnian Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Morgagnian Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Posterior Polar Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Posterior Polar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Membranous Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Membranous Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coronary Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coronary Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mature Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mature Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Coralliform Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coralliform Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Crystalline Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Crystalline Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absent Corpus Callosum Cataract Immunodeficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absent Corpus Callosum Cataract Immunodeficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Segment Anomalies And Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Segment Anomalies And Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Segment Anomalies With Or Without Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Segment Anomalies With Or Without Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Branchiootorenal Syndrome With Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Branchiootorenal Syndrome With Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lamellar Pulverulent Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lamellar Pulverulent Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Capsular Cataract (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Capsular Cataract (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atopic Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atopic Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cortical Pulverulent Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cortical Pulverulent Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Punctate Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Punctate Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticosteroid Induced Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticosteroid Induced Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Incipient Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Incipient Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mixed Type Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mixed Type Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Polar Cataract 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Polar Cataract 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Nuclear Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Nuclear Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Polar Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Polar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Iridescent Posterior Subcapsular Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iridescent Posterior Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Capsular Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Capsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Y-Sutural Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Y-Sutural Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dense Posterior Cortical Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dense Posterior Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Anterior Cortical Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Posterior Cortical Cataract Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nuclear cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nuclear cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
developmental cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the developmental cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
total cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the total cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
subcapsular cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the subcapsular cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
posterior subcapsular cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior subcapsular cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cortical cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anterior subcapsular cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anterior subcapsular cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anterior polar cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anterior polar cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lamellar cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lamellar cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
anterior cortical cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the anterior cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
polar cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the polar cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
posterior cortical cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
mature cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the mature cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
sutural cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sutural cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
immature cataract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the immature cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cataract Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the cataract phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Cataract Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cataract from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
hyperferritinemia-cataract syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease hyperferritinemia-cataract syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 18 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 18 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Senile cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mature cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
hyperferritinemia-cataract syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease hyperferritinemia-cataract syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 9 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 9 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Posterior polar cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polar cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 37 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 37 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Morgagni cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Morgagni cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Immature cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Immature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 8 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 8 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 6 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 6 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 1 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 1 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 32 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 32 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 13 with adult i phenotype Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 13 with adult i phenotype in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cortical senile cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cortical senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 4 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 4 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 11 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 11 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 10 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 10 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 3 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 3 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 21 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 21 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 28 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 28 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 31 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 31 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nuclear senile cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nuclear senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myotonic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myotonic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 14 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 14 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 34 multiple types Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 34 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tetanic cataract Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tetanic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cataract 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 12 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 12 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 1 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 1 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Aculeiform cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Aculeiform cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 4 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 4 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 3 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 3 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 9 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 9 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypomyelination and Congenital Cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Porencephaly-microcephaly-bilateral congenital cataract syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Porencephaly-microcephaly-bilateral congenital cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 16 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 16 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 39 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 39 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 14 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 14 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 15 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 15 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 10 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 10 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 34 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 34 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 11 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 11 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Zonular Pulverulent Cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Zonular Pulverulent Cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 6 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 6 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 13 with adult I phenotype Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 13 with adult I phenotype phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 5 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 5 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 21 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 21 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital nuclear cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital nuclear cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 22 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 22 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Age-related cortical cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Age-related cortical cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 19 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 19 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 17 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 17 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cortical pulverulent cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cortical pulverulent cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nuclear pulverulent cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nuclear pulverulent cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 20 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 20 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 31 multiple Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 31 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Juvenile cataract-microcornea-renal glucosuria syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Juvenile cataract-microcornea-renal glucosuria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract 46 juvenile-onset Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract 46 juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset anterior polar cataract Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset anterior polar cataract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
lateral terminal nucleus of the accessory optic tract, lateral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral terminal nucleus of the accessory optic tract, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
lateral terminal nucleus of the accessory optic tract, ventral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral terminal nucleus of the accessory optic tract, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
dorsal terminal nucleus of the accessory optic tract Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in dorsal terminal nucleus of the accessory optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Superior colliculus, optic layer Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Superior colliculus, optic layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Nucleus of the optic tract Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral terminal nucleus of the accessory optic tract Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral terminal nucleus of the accessory optic tract relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
optic fiber layer of SC Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in optic fiber layer of SC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Coloboma of optic disc Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coloboma of optic disc phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic nerve hypoplasia, bilateral Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic nerve hypoplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic nerve aplasia, bilateral Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic nerve aplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Septo-optic dysplasia sequence Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Septo-optic dysplasia sequence phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Optic Neuritis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Neuritis from the curated CTD Gene-Disease Associations dataset.
Optic Atrophies, Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophies, Hereditary from the curated CTD Gene-Disease Associations dataset.
Optic Nerve Hypoplasia, Bilateral Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Nerve Hypoplasia, Bilateral from the curated CTD Gene-Disease Associations dataset.
Polymicrogyria With Optic Nerve Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Polymicrogyria With Optic Nerve Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Optic Nerve Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Nerve Diseases from the curated CTD Gene-Disease Associations dataset.
Cavitary Optic Disc Anomalies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cavitary Optic Disc Anomalies from the curated CTD Gene-Disease Associations dataset.
Coloboma of optic nerve Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Coloboma of optic nerve from the curated CTD Gene-Disease Associations dataset.
Optic Neuropathy, Ischemic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Neuropathy, Ischemic from the curated CTD Gene-Disease Associations dataset.
Optic Disk Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Optic Disk in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Optic Nerve Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Optic Nerve in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
toxic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease toxic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic nerve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic nerve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic nerve neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic nerve neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic papillitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic papillitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
leber hereditary optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leber hereditary optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic disk drusen Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic disk drusen in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic neuritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic neuritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic nerve sheath meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic nerve sheath meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic nerve glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic nerve glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple sclerosis; optic neuritis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis; optic neuritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leber's hereditary optic neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease leber's hereditary optic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic nerve diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic disk Gene Set From GAD Gene-Disease Associations genes associated with the disease optic disk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic nerve Gene Set From GAD Gene-Disease Associations genes associated with the disease optic nerve in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis Gene Set From GAD Gene-Disease Associations genes associated with the disease brain ischemia; giant cell arteritis; optic neuritis; temporal arteritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic nerve malformation Gene Set From GAD Gene-Disease Associations genes associated with the disease optic nerve malformation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; optic neuropathy, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; optic neuropathy, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term optic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
optic nerve development Gene Set From GO Biological Process Annotations 2015 genes participating in the optic nerve development biological process from the curated GO Biological Process Annotations 2015 dataset.
optic nerve morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the optic nerve morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
optic vesicle morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the optic vesicle morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
optic placode formation Gene Set From GO Biological Process Annotations 2015 genes participating in the optic placode formation biological process from the curated GO Biological Process Annotations 2015 dataset.
optic cup morphogenesis involved in camera-type eye development Gene Set From GO Biological Process Annotations 2015 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of optic nerve formation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of optic nerve formation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of optic nerve formation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of optic nerve formation biological process from the curated GO Biological Process Annotations 2015 dataset.
optic cup structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the optic cup structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
optic nerve structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the optic nerve structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
closure of optic fissure Gene Set From GO Biological Process Annotations 2015 genes participating in the closure of optic fissure biological process from the curated GO Biological Process Annotations 2015 dataset.
optic cup formation involved in camera-type eye development Gene Set From GO Biological Process Annotations 2015 genes participating in the optic cup formation involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2015 dataset.
optic placode formation involved in camera-type eye formation Gene Set From GO Biological Process Annotations 2015 genes participating in the optic placode formation involved in camera-type eye formation biological process from the curated GO Biological Process Annotations 2015 dataset.
optic chiasma development Gene Set From GO Biological Process Annotations 2015 genes participating in the optic chiasma development biological process from the curated GO Biological Process Annotations 2015 dataset.
Optic nerve measurement (rim area) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Optic nerve measurement (rim area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Optic nerve measurement (cup area) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Optic nerve measurement (cup area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Optic nerve measurement (disc area) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Optic nerve measurement (disc area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Optic nerve measurement (cup-to-disc ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Optic nerve measurement (cup-to-disc ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Optic disc parameters Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Optic disc parameters phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
optic nerve disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease optic nerve disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
optic nerve coloboma Gene Set From HPO Gene-Disease Associations genes associated with the optic nerve coloboma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the optic nerve Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic disc hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the optic disc hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic disc drusen Gene Set From HPO Gene-Disease Associations genes associated with the optic disc drusen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the optic disc Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the optic disc phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic disc pallor Gene Set From HPO Gene-Disease Associations genes associated with the optic disc pallor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic nerve dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the optic nerve dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the optic tract Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonarteritic anterior ischemic optic neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the nonarteritic anterior ischemic optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the optic tract Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic nerve compression Gene Set From HPO Gene-Disease Associations genes associated with the optic nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retrobulbar optic neuritis Gene Set From HPO Gene-Disease Associations genes associated with the retrobulbar optic neuritis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic nerve hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the optic nerve hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
septo-optic dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the septo-optic dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic glioma Gene Set From HPO Gene-Disease Associations genes associated with the optic glioma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic neuritis Gene Set From HPO Gene-Disease Associations genes associated with the optic neuritis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the optic nerve Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Optic Neuritis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Neuritis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Septo-Optic Dysplasia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Septo-Optic Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophies, Hereditary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophies, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Nerve Glioma Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Nerve Glioma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Disk Drusen Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Disk Drusen phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Nerve Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Nerve Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Neuropathy, Ischemic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Neuropathy, Ischemic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal optic disc morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic disc morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic stalk morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic stalk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent optic tract Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent optic tract phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent optic placodes Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent optic placodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve coloboma Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic tract morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic neuropathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic neuropathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic placode morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic placode morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic nerve innervation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic nerve innervation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent optic nerve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent optic nerve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic nerve morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic cup morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic cup morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic chiasm morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic chiasm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve swelling Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve swelling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic vesicle formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic vesicle formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic fissure morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic fissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent optic vesicle Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent optic vesicle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic fissure closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve cupping Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve cupping phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent optic disc Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent optic disc phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed optic fissure closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
enlarged optic nerve Gene Set From MPO Gene-Phenotype Associations gene mutations causing the enlarged optic nerve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic disc coloboma Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic disc coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic choroid morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic choroid morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic eminence morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic eminence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent optic chiasm Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent optic chiasm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve hypoplasia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic pit morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic pit morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal optic canal morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal optic canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set From OMIM Gene-Disease Associations genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
optic nerve hypoplasia and abnormalities of the central nervous system Gene Set From OMIM Gene-Disease Associations genes associated with the optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated OMIM Gene-Disease Associations dataset.
cavitary optic disc anomalies Gene Set From OMIM Gene-Disease Associations genes associated with the cavitary optic disc anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.
{nonarteritic anterior ischemic optic neuropathy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {nonarteritic anterior ischemic optic neuropathy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
coloboma of optic nerve Gene Set From OMIM Gene-Disease Associations genes associated with the coloboma of optic nerve phenotype from the curated OMIM Gene-Disease Associations dataset.
polymicrogyria with optic nerve hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the polymicrogyria with optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
optic nerve hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
optic cup Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue optic cup in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
optic ganglion Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue optic ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
optic nerve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue optic nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
optic lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue optic lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Coloboma Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Coloboma Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arteritic Anterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arteritic Anterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonarteritic Anterior Ischemic Optic Neuropathy (Naion) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonarteritic Anterior Ischemic Optic Neuropathy (Naion) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Nerve Oedema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Nerve Oedema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Septo-Optic Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Septo-Optic Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Neuritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Neuritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Nerve Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Nerve Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bilateral Optic Neuritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Optic Neuritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Optic Neuritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Optic Neuritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Nere Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Nere Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Nerve Aplasia, Bilateral Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Nerve Aplasia, Bilateral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Neuropathy, Ischemic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Neuropathy, Ischemic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Nerve Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Nerve Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Anomalies With Retinal And/Or Macular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Anomalies With Retinal And/Or Macular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporal Pallor Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporal Pallor Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disk Drusen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disk Drusen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Arteritic Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Arteritic Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cavitary Optic Disc Anomalies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cavitary Optic Disc Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Structural Anomaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Structural Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Perineuritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Perineuritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inherited Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inherited Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymicrogyria With Optic Nerve Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymicrogyria With Optic Nerve Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Disc Neovascularization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Disc Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pit Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pit Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meningioma Of Optic Nerve Sheath Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meningioma Of Optic Nerve Sheath in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Optic Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Optic Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Optic Disc Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Nerve Dysplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Nerve Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Compression Of Optic Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Compression Of Optic Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of Optic Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of Optic Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Nerve Misrouting Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Nerve Misrouting in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Nerve Pallor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Nerve Pallor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Optic Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Optic Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
optic vesicle morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the optic vesicle morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
optic nerve morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the optic nerve morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
closure of optic fissure Gene Set From GO Biological Process Annotations 2023 genes participating in the closure of optic fissure biological process from the curated GO Biological Process Annotations 2023 dataset.
optic cup morphogenesis involved in camera-type eye development Gene Set From GO Biological Process Annotations 2023 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2023 dataset.
optic nerve development Gene Set From GO Biological Process Annotations 2023 genes participating in the optic nerve development biological process from the curated GO Biological Process Annotations 2023 dataset.
optic nerve structural organization Gene Set From GO Biological Process Annotations 2023 genes participating in the optic nerve structural organization biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of optic nerve formation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of optic nerve formation biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of optic nerve formation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of optic nerve formation biological process from the curated GO Biological Process Annotations 2023 dataset.
MEIS1-26253404-OPTIC-CUPS-MOUSE Gene Set From ChEA Transcription Factor Targets 2022 target genes of the MEIS1-26253404-OPTIC-CUPS-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
abnormal optic cup morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic cup morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent optic vesicle Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic vesicle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic fissure closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic fissure closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed optic fissure closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed optic fissure closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic nerve morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic nerve morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic vesicle formation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic vesicle formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic stalk morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic stalk morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent optic pit Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic pit phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent optic placodes Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic placodes phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent optic nerve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic nerve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic nerve innervation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic nerve innervation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic placode morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic placode morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve hypoplasia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve coloboma Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve coloboma phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic choroid morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic choroid morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic canal morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic tract morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic tract morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent optic chiasm Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic chiasm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic disk coloboma Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic disk coloboma phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic disk morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic disk morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased optic chiasm size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased optic chiasm size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic chiasm morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic chiasm morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic eminence morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic eminence morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic pit morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic pit morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent optic tract Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic tract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased optic chiasm size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased optic chiasm size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
enlarged optic nerve Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged optic nerve phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic fissure morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal optic fissure morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic canal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic canal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent optic disk Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic disk phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve cupping Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve cupping phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic neuropathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic neuropathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve swelling Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve swelling phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent optic cup Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent optic cup phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal optic disk morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal optic disk morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
absent optic nerve Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the absent optic nerve phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal optic vesicle formation Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal optic vesicle formation phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
abnormal optic nerve morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal optic nerve morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
optic vesicle morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the optic vesicle morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
optic nerve morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the optic nerve morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
closure of optic fissure Gene Set From GO Biological Process Annotations 2025 genes participating in the closure of optic fissure biological process from the curated GO Biological Process Annotations 2025 dataset.
optic cup morphogenesis involved in camera-type eye development Gene Set From GO Biological Process Annotations 2025 genes participating in the optic cup morphogenesis involved in camera-type eye development biological process from the curated GO Biological Process Annotations 2025 dataset.
optic nerve development Gene Set From GO Biological Process Annotations 2025 genes participating in the optic nerve development biological process from the curated GO Biological Process Annotations 2025 dataset.
optic nerve structural organization Gene Set From GO Biological Process Annotations 2025 genes participating in the optic nerve structural organization biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of optic nerve formation Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of optic nerve formation biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of optic nerve formation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of optic nerve formation biological process from the curated GO Biological Process Annotations 2025 dataset.
Leber hereditary optic neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Leber hereditary optic neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Optic nerve disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Optic nerve disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
deafness-dystonia-optic neuronopathy syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease deafness-dystonia-optic neuronopathy syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Optic nerve disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Optic nerve disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Leber hereditary optic neuropathy and dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber hereditary optic neuropathy and dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bilateral optic nerve hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bilateral optic nerve hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic nerve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic nerve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leber hereditary optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber hereditary optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic neuritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic neuritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-arteritic anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-arteritic anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Toxic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Toxic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
deafness-dystonia-optic neuronopathy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease deafness-dystonia-optic neuronopathy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic papillitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic papillitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune optic neuritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune optic neuritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arteritic anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arteritic anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nutritional optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nutritional optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic disk drusen Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic disk drusen in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic nerve glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic nerve glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic nerve neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic nerve neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic nerve sheath meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic nerve sheath meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic disc anomalies with retinal and/or macular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic disc anomalies with retinal and/or macular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Coloboma of optic nerve Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Coloboma of optic nerve in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic nerve astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic nerve astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood optic nerve glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood optic nerve glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic nerve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Optic nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Optic lobe Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Optic lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Optic cup Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Optic cup in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Optic ganglion Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Optic ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Optic nerve glioma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic nerve glioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Isolated optic nerve hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Isolated optic nerve hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonarteritic anterior ischemic optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonarteritic anterior ischemic optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Septo-optic dysplasia sequence Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Septo-optic dysplasia sequence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic nerve hypoplasia and abnormalities of the central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Foveal hypoplasia 2 and optic nerve misrouting Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Foveal hypoplasia 2 and optic nerve misrouting phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal optic nerve morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal optic nerve morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial cavitary optic disk anomaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial cavitary optic disk anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leber-like hereditary optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber-like hereditary optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leber hereditary optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber hereditary optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Coloboma of optic nerve Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Coloboma of optic nerve phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic cup area Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic cup area phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic disc area Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic disc area phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic disc size Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic disc size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic nerve head parameters (multi-trait analysis) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic nerve head parameters (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic disc parameters Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic disc parameters phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic nerve measurement (cup area) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic nerve measurement (cup area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic nerve measurement (rim area) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic nerve measurement (rim area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic nerve measurement (disc area) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic nerve measurement (disc area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic nerve measurement (cup-to-disc ratio) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic nerve measurement (cup-to-disc ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Open-angle glaucoma and optic cup area Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Open-angle glaucoma and optic cup area phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Optic disc radius Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic disc radius phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy, Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset.
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.
skin atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrophy of testis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary choroidal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
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.
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.
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.
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.
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.
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.
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.
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.
dermal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the dermal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripapillary chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the frontal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcortical cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse skin atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor neuron atrophy Gene Set From HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pelvic girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pelvic girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
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.
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.
Muscular Atrophy, Spinal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.

Harmonizome 3.0

OPA6 Gene

OPA4 Gene

OPA5 Gene

OPA2 Gene

OPA1 Gene

OPA3 Gene

SPOAN Gene

LOAS Gene

CODA Gene

GUST Gene

PBCRA1 Gene

CLAM Gene

SMAR Gene

SMAL Gene

SCA18 Gene

SMAJ Gene

optic atrophy 3 with cataract Gene Set

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

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

Optic atrophy and cataract, autosomal dominant Gene Set

Optic atrophy and cataract, autosomal dominant Gene Set

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

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

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

Optic Atrophy Type 1 Gene Set

Hereditary motor and sensory neuropathy with optic atrophy Gene Set

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

Optic Atrophy, Hereditary, Leber Gene Set

Optic atrophy 1 and deafness Gene Set

Optic Atrophy 7 Gene Set

Optic Atrophy 4 Gene Set

Optic atrophy 5 Gene Set

Costeff optic atrophy syndrome Gene Set

Optic atrophy polyneuropathy deafness Gene Set

Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set

Optic atrophy 6 Gene Set

Optic Atrophy Gene Set

OPTIC ATROPHY 2 Gene Set

Optic Atrophy, Autosomal Dominant Gene Set

primary optic atrophy Gene Set

partial optic atrophy Gene Set

optic atrophy Gene Set

optic disc atrophy Gene Set

optic atrophy Gene Set

blindness; optic atrophy, hereditary, leber Gene Set

optic atrophy, hereditary, leber Gene Set

optic atrophy, hereditary, leber; vision disorders Gene Set

optic atrophy and moderate deafness Gene Set

optic atrophy Gene Set

leber optic atrophy Gene Set

optic atrophy from cranial nerve compression Gene Set

Optic Atrophy, Hereditary, Leber Gene Set

Optic Atrophy, Autosomal Dominant Gene Set

Optic Atrophy Gene Set

Optic atrophy 3-like Gene Set

optic nerve atrophy Gene Set

optic atrophy 6 Gene Set

optic atrophy 5 Gene Set

optic atrophy 1 Gene Set

optic atrophy-4 Gene Set

optic atrophy-7 Gene Set

spastic paraplegia, optic atrophy, and neuropathy Gene Set

bosch-boonstra-schaaf optic atrophy syndrome Gene Set

optic atrophy 2, x-linked Gene Set

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

?neurodegeneration with optic atrophy, childhood onset Gene Set

optic atrophy plus syndrome Gene Set

{leber optic atrophy, susceptibility to} Gene Set

Optic Atrophy Gene Set

Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene Set

Atrophy Of Optic Disc Gene Set

Dominant Hereditary Optic Atrophy Gene Set

Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set

Auditory Neuropathy And Optic Atrophy Gene Set