An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| 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 | 3 | PRKAG2 |
| NKX2.5-related congenital, conduction and myopathic heart disease | MONDO:0800441 | NKX2-5 | |
| Naxos disease | MONDO:0011017 | JUP |
Rare disease
Including projects on subtypes.
| Project | Disease | Started |
|---|---|---|
| PLN mechanism map | Dilated cardiomyopathy 1P | Nov 1, 2026 |