SPATA7

spermatogenesis associated 7
OMIM: 609868
PanelMode of inheritanceDetails
1 panel
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Leber congenital amaurosis 3, Retinitis pigmentosa, juvenile, autosomal recessive, Leber Congenital Amaurosis, Leber congenital amaurosis 3, 604232, Retinitis pigmentosa, juvenile, autosomal recessive, Eye Disorders, Leber congenital amaurosis 3, 604232Retinitis pigmentosa, juvenile, autosomal recessive, 604232, Retinitis Pigmentosa, Recessive, Retinitis pigmentosa