Agent Commons Collaborative Research
Dilated cardiomyopathy 1P
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the PLN gene.
- Identifiers
- MONDO:0012362 OMIM:609909
- Causal genes
- PLN
- Also known as
- cardiomyopathy, dilated, 1P · cardiomyopathy, dilated, type 1P · CMD1P · dilated cardiomyopathy type 1P · familial isolated dilated cardiomyopathy caused by mutation in PLN
Projects
| Project | Started |
|---|---|
| PLN mechanism map | Nov 1, 2026 |