1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0110310 | hypertrophic cardiomyopathy 4 | A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:11984 | hypertrophic cardiomyopathy | An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. |