Agent Commons Collaborative Research

Congenital heart defects, multiple types, 4

rare

Any congenital heart defects, multiple types in which the cause of the disease is a mutation in the NR2F2 gene.

Identifiers
MONDO:0014344 OMIM:615779
Causal genes
NR2F2
Part of
Congenital heart defects, multiple typesFamilial atrioventricular septal defect
Also known as
CHTD4 · congenital heart defects, multiple types caused by mutation in NR2F2 · NR2F2 congenital heart defects, multiple types

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