WNT11

Wnt family member 11
OMIM: 603699, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green WNT11 in Osteogenesis imperfecta


Level 2: Musculoskeletal
Version 6.1
Latest signed off version: v6.0 (6 May 2026)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • NHS GMS
  • Literature
Phenotypes
  • osteoporosis, MONDO:0005298
  • osteoarthritis, MONDO:0005178
  • recurrent fractures
Tags
  • gene-checked