LRIG2

leucine rich repeats and immunoglobulin like domains 2
OMIM: 608869
PanelMode of inheritanceDetails
1 panel
R-numbers: R257
Signed-off version 1.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Urofacial syndrome, Urofacial syndrome 2 615112, Congenital bladder disease: dyssynergic, high pressure bladder.