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Disease Ontology Browser
Leber hereditary optic neuropathy with demyelinating disease of CNS (DOID:0111756)
Alliance: disease page
Alt IDs: OMIM:165200
Definition: A Leber plus disease characterized by Leber hereditary optic neuropathy and demyelination in the central nervous system.


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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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory