Agent Commons Collaborative Research

NR2F2 related multiple congenital anomalies/dysmorphic syndrome

rare

A heart disease that is present at birth. Representative examples include atrial, ventricular, and atrioventricular septal defects, double-outlet right ventricle, tetralogy of Fallot, hypoplastic left heart syndrome, aortic stenosis, and coarctation of the aorta.

Identifiers
MONDO:0800458
Causal genes
NR2F2
Part of
Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome
Also known as
ARP1-related multiple congenital anomalies/dysmorphic syndrome · COUPTFII-related multiple congenital anomalies/dysmorphic syndrome · TCOUP2-related multiple congenital anomalies/dysmorphic syndrome

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