CFC1

cripto, FRL-1, cryptic family 1
OMIM: 605194
PanelMode of inheritanceDetails
2 panels
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CFC1-RELATED CONOTRUNCAL HEART MALFORMATIONS, Heterotaxy, visceral, 2, autosomal, 605376
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 1.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Heterotaxy, visceral, 2, autosomal 605376