LRAT

lecithin retinol acyltransferase
OMIM: 604863
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Leber congenital amaurosis 14, Retinal dystrophy, early - onset severe, Retinitis pigmentosa, juvenile, Leber Congenital Amaurosis, Retinal dystrophy, early-onset severe, 613341, Retinitis pigmentosa, Retinitis Pigmentosa, Recessive, Eye Disorders