CLMP

CXADR like membrane protein
OMIM: 611693
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
CONGENITAL SHORT BOWEL SYNDROME 615237
R-numbers: R331
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Congenital short bowel syndrome, OMIM:615237