SPATA7

spermatogenesis associated 7
OMIM: 609868
PanelMode of inheritanceDetails
1 panel
R-numbers: R32, R33, R34, R35
Signed-off version 2.195
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