Optic Atrophy, Hereditary, Leber Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D029242
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Genes

8 genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MT-ND4 NADH dehydrogenase, subunit 4 (complex I) 2.88009
MT-ND6 NADH dehydrogenase, subunit 6 (complex I) 2.88009
LRAT lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase) 2.88009
IL1A interleukin 1, alpha 2.88009
IL1B interleukin 1, beta 2.88009
RPE65 retinal pigment epithelium-specific protein 65kDa 2.88009
LOAS Leber optic atrophy, susceptibility to 2.88009
ND1 2.88009