Genomics England
GMS Panels
Panels
Genes and Entities

WNT4

Wnt family member 4
OMIM: 603490
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
MULLERIAN APLASIA AND HYPERANDROGENISM 158330, SERKAL SYNDROME 611812