Genomics England
GMS Panels
Panels
Genes and Entities

WNT7B

Wnt family member 7B
OMIM: 601967
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
WNT7B-related PDAC syndrome
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Pulmonary hypoplasia, Diaphragmatic anomalies, Anophthalmia/Microphthalmia, Cardiac defects