| description | Protein which, if defective, causes Leber hereditary optic neuropathy, a mitochondrial disease leading to bilateral, painless loss of central vision due to selective degeneration of the retinal ganglion cells and their axons. The disease arises during young adult life and displays sex-dependent incomplete penetrance and male predominance |
Ontology Term --> All ancestors
Ontology Term --> All descendants
Ontology Term --> Direct children
Ontology Term --> Direct parents
