ADAM9

ADAM metallopeptidase domain 9
OMIM: 602713
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 5.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Achromatopsia, Cone, and Cone-rod Dystrophy, Eye Disorders, Cone-Rod Dystrophy, Recessive, Cone-rod dystrophy 9, 612775