CRELD1

cysteine rich with EGF like domains 1
OMIM: 607170
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
HETEROTAXY SYNDROME 207574