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

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

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Cardiogenetic disease (614) ↑ Congenital heart disease (416)

Including sub-types (73) Tagged with HAND2 related congenital heart defect (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.