| DISEASE NAME | NON RARE IN EUROPE: Familial isolated hypertrophic cardiomyopathy |
| DISEASE CATEGORY (ICD10) | Diseases of the circulatory system |
| DISEASE ID (ICD10) | I42.1 |
| DISEASE ID (OMIM) | N.A. |
| 2 combinations linked to 155 | OLI1327; OLI1794 |
| 2 gene combinations linked to 155 | COL6A1; LZTR1; TTN; MYH7; TPM1 |
| ORPHANET ID | 155 |