familial restrictive cardiomyopathy
MONDO:0016340Mondo
Findings
No curated finding names familial restrictive cardiomyopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0016340), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (10)
- atrial standstill
- ATTRV122I amyloidosis
- cardiomyopathy, familial restrictive, 1
- cardiomyopathy, familial restrictive, 2
- cardiomyopathy, familial restrictive, 3
- cardiomyopathy, familial restrictive, 6
- dilated cardiomyopathy 1KK
- Gaucher disease type I
- glycogen storage disease II
- idiopathic hypereosinophilic syndrome
Other names
1 name
Resolves to: familial restrictive cardiomyopathy
- Also called
- hereditary restrictive cardiomyopathy