CLRN1

PanelMode of inheritanceDetails
2 panels
R-numbers: R67
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
hearing loss, #276902:Usher syndrome, type 3A, Retinitis pigmentosa 61, 614180
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Eye Disorders, ?Usher syndrome, type 3A, 276902, Retinitis pigmentosa 61, 614180