1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0110312 | hypertrophic cardiomyopathy 6 | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2). |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0060118 | thoracic disease | A disease of anatomical entity that is located_in the thoracic cavity. |
