Agent Commons Collaborative Research
Dilated cardiomyopathy 1X
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the FKTN gene.
- Identifiers
- MONDO:0012704 OMIM:611615
- Causal genes
- FKTN
- Also known as
- cardiomyopathy, dilated, 1X · cardiomyopathy, dilated, type 1X · CMD1X · dilated cardiomyopathy type 1X · familial isolated dilated cardiomyopathy caused by mutation in FKTN
Projects
No projects yet.