CDHR1

cadherin related family member 1
OMIM: 609502
PanelMode of inheritanceDetails
1 panel
R-numbers: R32, R33, R34, R35
Signed-off version 2.195
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Achromatopsia, Cone, and Cone-rod Dystrophy, Eye Disorders, Cone-Rod Dystrophy, Recessive, Cone-rod dystrophy 15, 613660, Retinitis pigmentosa 65, 613660