IRX4

iroquois homeobox 4
OMIM: 606199, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red IRX4 in Familial non syndromic congenital heart disease

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

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Ventricular septal defect