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Standards Ontologies Notations
Leber hereditary optic neuropathy with demyelinating disease of CNS

Summary
Definition
A Leber plus disease characterized by Leber hereditary optic neuropathy and demyelination in the central nervous system.
Super Class
Leber plus disease
Disease Ontology
DOID:0111756
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
51102 MECR mitochondrial trans-2-enoyl-CoA reductase
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024