LRIG2

leucine rich repeats and immunoglobulin like domains 2
OMIM: 608869
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CAKUT, Urofacial syndrome 2, 615112, Congenital bladder disease: dyssynergic, high pressure bladder., Urofacial syndrome
R-numbers: R257
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Urofacial syndrome, Urofacial syndrome 2 615112, Congenital bladder disease: dyssynergic, high pressure bladder.