FGF4

fibroblast growth factor 4
OMIM: 164980, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FGF4 in Skeletal dysplasia


Level 2: Musculoskeletal
Version 8.34
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Short-rib thoracic dysplasia 22 without polydactyly, OMIM:621260
    • Jeune syndrome, MONDO:0018770
    Tags
    • Q3_25_promote_green