9 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:1287 | cardiovascular system disease | A disease of anatomical entity which occurs in the blood, heart, blood vessels or the lymphatic system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells or lymph to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis. |
| DOID:114 | heart disease | A cardiovascular system disease that involves the heart. |
| DOID:0060118 | thoracic disease | A disease of anatomical entity that is located_in the thoracic cavity. |
| DOID:0060036 | intrinsic cardiomyopathy | A cardiomyopathy that is characterized as weakness in the muscle of the heart that is not due to an identifiable external cause. |
| DOID:0050700 | cardiomyopathy | A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. |
| DOID:397 | restrictive cardiomyopathy | An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium. |
| DOID:0111426 | restrictive cardiomyopathy 2 | A restrictive cardiomyopathy that has_material_basis_in variation in a region on chromosome 10q23.3. |
8 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:397 | DOID:0111426 |
| is_a | DOID:0060036 | DOID:0111426 |
| is_a | DOID:7 | DOID:0111426 |
| is_a | DOID:1287 | DOID:0111426 |
| is_a | DOID:4 | DOID:0111426 |
| is_a | DOID:0050700 | DOID:0111426 |
| is_a | DOID:0060118 | DOID:0111426 |
| is_a | DOID:114 | DOID:0111426 |
