LCA5

LCA5, lebercilin
OMIM: 611408
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 5.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Leber congenital amaurosis 5, Leber Congenital Amaurosis, Leber congenital amaurosis 5, 604537, Eye Disorders, Leber congenital amaurosis 5