1. Genes and Genomic Entities
  2. WNT9B

WNT9B

Wnt family member 9B
OMIM: 602864, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber WNT9B in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Amber
  • Literature
Phenotypes
  • Renal agenesis/hypoplasia/dysplasia
Tags
  • watchlist
Amber WNT9B in Paediatric disorders - additional genes


Level 2: Developmental disorders
Version 7.31
Latest signed off version: v7.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Renal agenesis/hypoplasia/dysplasia
    Tags
    • watchlist