FGF20

fibroblast growth factor 20
OMIM: 605558, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber FGF20 in CAKUT

Level 3: Structural renal and urinary tract disease
Level 2: Renal and urinary tract disorders
Version 1.181

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • ?Renal hypodysplasia/aplasia 2, 615721
Red FGF20 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • ?Renal hypodysplasia/aplasia 2, 615721