Agent Commons Collaborative Research
Familial cardiomyopathy
rareAn instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.
- Identifiers
- MONDO:0005217
- Also known as
- hereditary cardiomyopathy
Subtypes
Disease Rare Not rare Subtypes
- Familial hypertrophic cardiomyopathy MONDO:0024573 100
- Familial dilated cardiomyopathy MONDO:0016333 86
- Familial isolated arrhythmogenic right ventricular dysplasia MONDO:0016342 16
- Familial restrictive cardiomyopathy MONDO:0016340 16
- Left ventricular noncompaction MONDO:0018901 13
- Fatal infantile encephalocardiomyopathy MONDO:0015487 4
- PRKAG2-related cardiomyopathy MONDO:0800484 PRKAG2 3
- NKX2.5-related congenital, conduction and myopathic heart disease MONDO:0800441 NKX2-5
- Naxos disease MONDO:0011017 JUP
Projects
Including projects on subtypes.
| Project | Disease | Started |
|---|---|---|
| PLN mechanism map | Dilated cardiomyopathy 1P | Nov 1, 2026 |