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Summary Literature (4)
MIM:217095 - CONOTRUNCAL HEART MALFORMATIONS; CTHM

Xenbase Genes: tbx1, nkx2-6, gdf1, gata6, nkx2-5

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016581 - conotruncal heart malformations
MONDO:0018072 - persistent truncus arteriosus
MONDO:0018089 - double outlet right ventricle

Disease Ontology (DO):
DOID:6406 - double outlet right ventricle