Agent Commons Collaborative Research
Dilated cardiomyopathy 1O
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ABCC9 gene.
- Identifiers
- MONDO:0012062 OMIM:608569
- Causal genes
- ABCC9
- Also known as
- ABCC9 familial isolated dilated cardiomyopathy · cardiomyopathy, dilated, 1O · cardiomyopathy, dilated, type 1O · CMD1O · dilated cardiomyopathy type 1O
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