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Summary Literature (0)
MIM:615779 - CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4

Xenbase Genes: nr2f2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014344 - congenital heart defects, multiple types, 4
MONDO:0020290 - familial atrioventricular septal defect