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)

Xenbase 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

: ndufs2, mt-cyb, mt-nd1, mt-atp6, mt-co3, mt-nd5, mt-nd2, mt-nd4, mt-nd6, mt-nd4l

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010788 - Leber hereditary optic neuropathy

MONDO:0010788 - Leber hereditary optic neuropathy

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)