leber optic atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Degeneration of retinal ganglion cells and their axons. (Human Phenotype Ontology, HP_0001112)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001112
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Genes

7 genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COX1
COX3
MT-CYB cytochrome b
MT-ND2 MTND2
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
ND1