familial cardiomyopathy
MONDO:0005217Mondo
Findings
No curated finding names familial cardiomyopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0005217), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
- Narrower terms (9)
- familial dilated cardiomyopathy
- familial hypertrophic cardiomyopathy
- familial isolated arrhythmogenic right ventricular dysplasia
- familial restrictive cardiomyopathy
- fatal infantile encephalocardiomyopathy
- left ventricular noncompaction
- Naxos disease
- NKX2.5-related congenital, conduction and myopathic heart disease
- PRKAG2-related cardiomyopathy
Other names
1 name
Resolves to: familial cardiomyopathy
- Also called
- hereditary cardiomyopathy