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DOID:0111755 - Leber hereditary optic neuropathy and dystonia
Disease Ontology Definition:A Leber plus disease characterized by Leber hereditary optic neuropathy and dystonia that has_material_basis_in mutation in the mitochondrial genes MTND6, MTND4, MTND1 or MTND3 that make up the mitochondrial complex I.
Synonyms: LDYT, Leber optic atrophy and dystonia, Leber optic atrophy with dystonia, Marsden syndrome, familial dystonia with visual failure and striatal lucencies,
Xenbase Genes
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Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Leber plus disease (is_a)