familial isolated dilated cardiomyopathy
ORPHA: 154
Overview
Familial isolated dilated cardiomyopathy is a rare, genetically heterogeneous cardiac disease characterized by dilatation leading to systolic and diastolic dysfunction of the left and/or right ventricles, causing heart failure or arrhythmia
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with familial isolated dilated cardiomyopathy, sourced from HPO and Orphanet clinical annotations.
Dilated cardiomyopathyLeft ventricular systolic dysfunctionEdemaCongestive heart failureExertional dyspneaArrhythmiaFatigueOrthopneaSensorineural hearing impairmentThromboembolic strokeMyopathyEMG abnormalityLipoatrophy
Classification & Codes
Orphanet Code
ORPHA:154familial isolated dilated cardiomyopathy
| Orphanet | ORPHA:154 |
| Treatments | 0 drug(s) |
| Symptoms on record | 13 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO