NR2F2 related multiple congenital anomalies/dysmorphic syndrome

MONDO:0800458

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.

Also known as: ARP1-related multiple congenital anomalies/dysmorphic syndrome, COUPTFII-related multiple congenital anomalies/dysmorphic syndrome, NR2F2 related multiple congenital anomalies/dysmorphic syndrome, TCOUP2-related multiple congenital anomalies/dysmorphic syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with NR2F2 related multiple congenital anomalies/dysmorphic syndrome itself.

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↑ Hereditary disease (18235) ↑ Multiple congenital anomalies/dysmorphic syndrome (289)

Including sub-types (0) Tagged with NR2F2 related multiple congenital anomalies/dysmorphic syndrome (0)

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