histiocytoid cardiomyopathy
MONDO:0010771Mondo
Findings
No curated finding names histiocytoid cardiomyopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Histiocytoid cardiomyopathy is an arrhythmogenic disorder characterized by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.
Definition from the Mondo Disease Ontology (MONDO:0010771), read 2026-09-29. CC BY 4.0.
Features
44 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- TachycardiaHPOHP:0001649
- Very frequent (80% to 99% of cases)
- Supraventricular tachycardiaHPOHP:0004755
- Frequent (30% to 79% of cases)
- Ventricular tachycardiaHPOHP:0004756
- Frequent (30% to 79% of cases)
- Atrioventricular blockHPOHP:0001678
- Occasional (5% to 29% of cases)
- CardiomegalyHPOHP:0001640
- Occasional (5% to 29% of cases)
- Complete right bundle branch blockHPOHP:0011712
- Occasional (5% to 29% of cases)
- Congestive heart failureHPOHP:0001635
- Occasional (5% to 29% of cases)
- CoughHPOHP:0012735
- Occasional (5% to 29% of cases)
- CyanosisHPOHP:0000961
- Occasional (5% to 29% of cases)
- DrowsinessHPOHP:0002329
- Occasional (5% to 29% of cases)
- Exercise intoleranceHPOHP:0003546
- Occasional (5% to 29% of cases)
- Failure to thriveHPOHP:0001508
- Occasional (5% to 29% of cases)
Show the remaining 32
- FeverHPOHP:0001945
- Occasional (5% to 29% of cases)
- HepatomegalyHPOHP:0002240
- Occasional (5% to 29% of cases)
- Junctional ectopic tachycardiaHPOHP:0011716
- Occasional (5% to 29% of cases)
- PallorHPOHP:0000980
- Occasional (5% to 29% of cases)
- Stroke-like episodeHPOHP:0002401
- Occasional (5% to 29% of cases)
- TachypneaHPOHP:0002789
- Occasional (5% to 29% of cases)
Where it sits
- Narrower terms (1)
Other names
9 names
Resolves to: histiocytoid cardiomyopathy
- Also called
- Arachnocytosis of the myocardiumcongenital cardiomyopathyfoamy myocardial transformation of infancyinfantile cardiomyopathy with histiocytoid changeinfantile xanthomatous cardiomyopathyisolated Cardiac lipidosismyocardial hamartomaoncocytic cardiomyopathyPurkinje cell hamartoma