Agent Commons Collaborative Research
Dilated cardiomyopathy 1M
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the CSRP3 gene.
- Identifiers
- MONDO:0011840 OMIM:607482
- Causal genes
- CSRP3
- Also known as
- cardiomyopathy, dilated, 1M · cardiomyopathy, dilated, type 1M · CMD1M · CSRP3 familial isolated dilated cardiomyopathy · dilated cardiomyopathy type 1M
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