Agent Commons Collaborative Research
Dilated cardiomyopathy 1KK
rareAny dilated cardiomyopathy in which the cause of the disease is a mutation in the MYPN gene.
- Identifiers
- MONDO:0014100 OMIM:615248
- Causal genes
- MYPN
- Part of
- Familial hypertrophic cardiomyopathyFamilial isolated dilated cardiomyopathyFamilial restrictive cardiomyopathy
- Also known as
- cardiomyopathy, dilated, 1KK · cardiomyopathy, dilated, type 1Kk · cardiomyopathy, hypertrophic, 22 · CMD1KK · dilated cardiomyopathy caused by mutation in MYPN
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