HAND2 related congenital heart defect

MONDO:0800476

A heart disease that is present at birth caused by a variation in th HAND2 gene. Representative examples include tetralogy of fallot and ventricular septal defect.

Also known as: DHAND, DHAND2, HAND2 related congenital heart defect, HAND2-related congenital heart defect, HLH transcription factor HAND2, Hed, Thing2, bHLHa26

75 clinical trials for this condition and its sub-types, 0 tagged with HAND2 related congenital heart defect itself.

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↑ Cardiogenetic disease (618) ↑ Congenital heart disease (419)

Including sub-types (75) Tagged with HAND2 related congenital heart defect (0)

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