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DOID:0111756 - Leber hereditary optic neuropathy with demyelinating disease of CNS
Disease Ontology Definition:A Leber plus disease characterized by Leber hereditary optic neuropathy and demyelination in the central nervous system.
Synonyms:
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)