Genomics England
GMS Panels
Panels
Genes and Entities

LRIG2

leucine rich repeats and immunoglobulin like domains 2
OMIM: 608869
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
UROFACIAL SYNDROME 236730
Green
in Paediatric disorders - additional genes
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.7
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CAKUT, Urofacial syndrome 2, 615112, Congenital bladder disease: dyssynergic, high pressure bladder., Urofacial syndrome
Green
in Unexplained young onset end-stage renal disease
R-numbers: R257
Signed-off version 3.11
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Urofacial syndrome, Urofacial syndrome 2 615112, Congenital bladder disease: dyssynergic, high pressure bladder.