FGFR4

fibroblast growth factor receptor 4
OMIM: 134935, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red FGFR4 in Heterotaxy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.1

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Visceral heterotaxy, MONDO:0018677, FGFR4-related

Red FGFR4 in Mendeliome


Version 2.76

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Visceral heterotaxy, MONDO:0018677, FGFR4-related