FOXL1

forkhead box L1
OMIM: 603252, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red FOXL1 in Familial non syndromic congenital heart disease

Level 3: Congenital heart disease
Level 2: Cardiovascular disorders
Version 1.80

review Not set
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Hypoplastic left heart syndrome (Iascone (2012) Clin Genet 81,542)