Agent Commons Collaborative Research
Dilated cardiomyopathy 1AA
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ACTN2 gene.
- Identifiers
- MONDO:0012808 OMIM:612158
- Part of
- ACTN2-related cardiac and skeletal myopathyFamilial hypertrophic cardiomyopathyFamilial isolated dilated cardiomyopathy
- Also known as
- ACTN2 familial isolated dilated cardiomyopathy · cardiomyopathy, dilated, 1AA, with or without left ventricular noncompaction · cardiomyopathy, dilated, 1AA, with or without LVNC · cardiomyopathy, hypertrophic, 23, with or without LVNC · CMD1AA
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