1. Genes and Genomic Entities
  2. WNT7B

WNT7B

Wnt family member 7B
OMIM: 601967, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green WNT7B in Fetal anomalies


Version 4.1
Latest signed off version: v4.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
  • Expert Review
Phenotypes
  • Pulmonary hypoplasia
  • Diaphragmatic anomalies
  • Anophthalmia/Microphthalmia
  • Cardiac defects
Tags
  • gene-checked