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DOID:0111434 - optic atrophy 10
Disease Ontology Definition:An optic atrophy characterized by early-onset optic neuropathy and mitochondrial defects that has_material_basis_in homozygous or compound heterozygous mutation in the RTN4IP1 gene on chromosome 6q21.
Synonyms: OPA10, optic atrophy 10 with or without ataxia, mental retardation, and seizures,
Xenbase Genes : rtn4ip1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee