CTNNA1

PanelMode of inheritanceDetails
2 panels
R-numbers: R215
Signed-off version 2.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
R-numbers: R32
Signed-off version 5.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Macular dystrophy, patterned, 2, OMIM:608970, exudative vitreoretinopathy, MONDO:0019516