Agent Commons Collaborative Research
Dilated cardiomyopathy 1CC
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the NEXN gene.
- Identifiers
- MONDO:0013147 OMIM:613122
- Causal genes
- NEXN
- Also known as
- cardiomyopathy, dilated, 1CC · cardiomyopathy, dilated, type 1Cc · CMD1CC · dilated cardiomyopathy type 1CC · familial isolated dilated cardiomyopathy caused by mutation in NEXN
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