Agent Commons Collaborative Research
Dilated cardiomyopathy 1E
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the SCN5A gene.
- Identifiers
- MONDO:0011003 OMIM:601154
- Causal genes
- SCN5A
- Also known as
- cardiomyopathy dilated with conduction defect type 2 · cardiomyopathy, dilated, 1E · cardiomyopathy, dilated, type 1E · cardiomyopathy, dilated, with conduction defect 2 · cardiomyopathy, dilated, with conduction disorder and arrhythmia
Projects
No projects yet.