RAX2

retina and anterior neural fold homeobox 2
OMIM: 610362
PanelMode of inheritanceDetails
1 panel
R-numbers: R32, R33, R34, R35
Signed-off version 2.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Achromatopsia, Cone, and Cone-rod Dystrophy, Macular Degeneration, Eye Disorders, Cone-Rod Dystrophy, Dominant, Cone-rod dystrophy 11