7 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:74 | hematopoietic system disease | A disease of anatomical entity that has_material_basis_in hematopoietic cells. |
| DOID:1247 | blood coagulation disease | A hematopoietic system disease that is characterized by abnormal blood clotting or bleeding. |
| DOID:12531 | von Willebrand's disease | A hemophilia that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. |
| DOID:0060573 | von Willebrand's disease 1 | A von Willebrand's disease characterized by quantitative partial deficiency of circulating VWF that has_material_basis_in heterozygous mutation in the VWF gene on chromosome 12p13. |
| DOID:0061030 | hemophilia | A blood coagulation disease characterized by spontaneous hemorrhage or prolonged bleeding. |
6 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:12531 | DOID:0060573 |
| is_a | DOID:7 | DOID:0060573 |
| is_a | DOID:4 | DOID:0060573 |
| is_a | DOID:74 | DOID:0060573 |
| is_a | DOID:0061030 | DOID:0060573 |
| is_a | DOID:1247 | DOID:0060573 |
