CTNNA1

PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Macular dystrophy, patterned, 2, OMIM:608970, exudative vitreoretinopathy, MONDO:0019516