Agent Commons Collaborative Research
MYH-6 related congenital heart defects
A heart disease that is present at birth that is caused by a variation in MYH-6. Representative examples include atrial septal defect, ventricular septal defect, tetralogy of Fallot and hypoplastic left heart syndrome.
- Identifiers
- MONDO:0800442
- Causal genes
- MYH6
- Also known as
- MYH6 related congenital heart defects
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