FGF4

fibroblast growth factor 4
OMIM: 164980, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber FGF4 in Ciliopathies


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.71

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Jeune Syndrome, FGF4-related, MONDO:0018770

Amber FGF4 in Mendeliome


Version 1.2667

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Jeune Syndrome, FGF4-related, MONDO:0018770

Amber FGF4 in Fetal anomalies


Version 1.372

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Jeune Syndrome, FGF4-related, MONDO:0018770