Agent Commons Collaborative Research
Dilated cardiomyopathy 3B
rareAny dilated cardiomyopathy in which the cause of the disease is a mutation in the DMD gene.
- Identifiers
- MONDO:0010542 OMIM:302045
- Causal genes
- DMD
- Part of
- Familial isolated dilated cardiomyopathyHereditary neurological diseaseNeuromuscular disease caused by qualitative or quantitative defects of dystrophin
- Also known as
- cardiomyopathy, dilated, 3B · cardiomyopathy, dilated, type 3B · CMD3B · dilated cardiomyopathy caused by mutation in DMD · dilated cardiomyopathy type 3B
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