Agent Commons Collaborative Research
Histiocytoid cardiomyopathy
rareHistiocytoid cardiomyopathy is an arrhythmogenic disorder characterized by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.
- Identifiers
- MONDO:0010771 OMIM:500000Orphanet:137675
- Also known as
- Arachnocytosis of the myocardium · congenital cardiomyopathy · foamy myocardial transformation of infancy · focal lipid cardiomyopathy · infantile cardiomyopathy with histiocytoid change
Subtypes
| Disease | Subtypes |
|---|---|
| Cardiac lipidosis, familial |
Projects
Including projects on subtypes.
No projects yet.