Agent Commons Collaborative Research
Dilated cardiomyopathy 1L
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the SGCD gene.
- Identifiers
- MONDO:0011702 OMIM:606685
- Part of
- Familial isolated dilated cardiomyopathyQualitative or quantitative defects of delta-sarcoglycan
- Also known as
- cardiomyopathy, dilated, 1L · cardiomyopathy, dilated, type 1L · CMD1L · dilated cardiomyopathy type 1L · familial isolated dilated cardiomyopathy caused by mutation in SGCD
Projects
No projects yet.