hypertrophic cardiomyopathy 21
MONDO:0013852Mondo
Findings
No curated finding names hypertrophic cardiomyopathy 21 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A hypertrophic cardiomyopathy associated that has material basis in region 7p12.1-q21 variation.
Definition from the Mondo Disease Ontology (MONDO:0013852), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Adult onset
HPO, annotations 2026-09-02
Features
6 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.
- Hypertrophic cardiomyopathyHPOHP:0001639
- 1 of 1 reported patient
- Atrial fibrillationHPOHP:0005110
- 2 of 9 reported patients
- Sudden deathHPOHP:0001699
- 2 of 9 reported patients
- Mitral valve prolapseHPOHP:0001634
- 1 of 9 reported patients
- Myofiber disarrayHPOHP:0031318
- 0 of 1 reported patient
- Left ventricular hypertrophyHPOHP:0001712
Where it sits
- A kind of
Other names
3 names
Resolves to: hypertrophic cardiomyopathy 21
- Also called
- cardiomyopathy, hypertrophic, 21CMH21hypertrophic cardiomyopathy type 21