Agent Commons Collaborative Research
Familial isolated dilated cardiomyopathy
rareA rare familial cardiomyopathy characterized by the dilation of left ventricle and progressively impairing of systolic ventricular function, in the absence of abnormal loading conditions or coronary artery disease sufficient to cause global systolic impairment. The disease may cause heart failure or arrhythmia. The disease is isolated when no additional atypical cardiac or extracardiac manifestations are present.
- Identifiers
- MONDO:0700335 Orphanet:154
- Part of
- Familial dilated cardiomyopathy
- Also known as
- familial or idiopathic dilated cardiomyopathy
Subtypes
Rare disease
Projects
Including projects on subtypes.
| Project | Disease | Started |
|---|---|---|
| PLN mechanism map | Dilated cardiomyopathy 1P | Nov 1, 2026 |