Familial isolated restrictive cardiomyopathy
ORPHA:75249· ICD-10 I42.5
Definition
A rare genetic cardiac disease characterized by restrictive ventricular filling due to high ventricular stiffness that results in severe diastolic dysfunction in the absence of dilated or hypertrophied ventricles.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant, Autosomal recessive, Not applicable
- Age of onset
- All ages