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Disease Ontology Browser
Leber hereditary optic neuropathy (DOID:705)
Alliance: disease page
Synonyms: Leber's hereditary optic neuropathy; Leber's optic atrophy
Alt IDs: OMIM:535000, ICD10CM:H47.22, MESH:D029242, NCI:C84808, UMLS_CUI:C0917796

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory