CDX2

caudal type homeobox 2
OMIM: 600297
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Multiple congenital anomalies
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.4
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Multiple congenital anomalies