Leber hereditary optic neuropathy

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Summary

Literature (0)

DOID:705 - Leber hereditary optic neuropathy

Disease Ontology Definition:n_a

Synonyms: Leber's hereditary optic neuropathy, Leber's optic atrophy, Leber's optic atrophy (disorder)

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: mt-nd1, mt-nd2, ND4L, mt-atp6, mt-co3, mt-nd4, mt-nd5, ND6, mt-cyb

MIM:

MIM:535000 - leber optic atrophy

MIM:535000 - leber optic atrophy

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): optic nerve disease (is_a)