Agent Commons Collaborative Research
Coronary artery disease, autosomal dominant, 1
Any coronary artery disease in which the cause of the disease is a mutation in the MEF2A gene.
- Identifiers
- MONDO:0012011 OMIM:608320
- Causal genes
- MEF2A
- Also known as
- ADCAD1 · coronary artery disease caused by mutation in MEF2A · coronary artery disease, autosomal dominant, type 1 · MEF2A coronary artery disease
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