FGD5

FYVE, RhoGEF and PH domain containing 5
OMIM: 614788, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FGD5 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.26
Latest signed off version: v8.0 (12 Aug 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • NHS GMS
  • Expert Review Amber
Phenotypes
  • Congenital heart disease, tetralogy of Fallout (TOF), peripheral pulmonary artery stenosis (PPS)