RD3

retinal degeneration 3
OMIM: 180040
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Leber Congenital Amaurosis, Leber congenital amaurosis 12, 610612, Eye Disorders