WNT9B

Wnt family member 9B
OMIM: 602864, Gene2Phenotype

2 panels

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


Version 3.157
Latest signed off version: v3.0 (22 Mar 2023)

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


Version 3.10
Latest signed off version: v3.0 (22 Mar 2023)

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