RAX2

retina and anterior neural fold homeobox 2
OMIM: 610362
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 7.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Cone-rod dystrophy 11, OMIM:610381, Retinitis pigmentosa 95, OMIM:620102, ?Macular degeneration, age-related, 6, OMIM:613757