14 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:178 | vascular disease | A cardiovascular system disease that primarily affects the blood vessels which includes the arteries, veins and capillaries that carry blood to and from the heart. |
| 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:863 | nervous system disease | A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. |
| DOID:936 | brain disease | A central nervous system disease that is located_in the brain. |
| DOID:331 | central nervous system disease | A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system. |
| DOID:0050828 | artery disease | A vascular disease that is located_in an artery. |
| DOID:10941 | intracranial aneurysm | |
| DOID:0060228 | intracranial berry aneurysm | An intracranial aneurysm with a characteristic rounded shape; the most common form of cerebral aneurysm. |
| DOID:3527 | cerebral arterial disease | |
| DOID:13089 | intracranial arterial disease | |
| DOID:6713 | cerebrovascular disease | An vascular disease that is characterized by dysfunction of the blood vessels supplying the brain. |
| DOID:0080975 | intracranial berry aneurysm 12 | An intracranial berry aneurysm that is characterized by rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death and that has_material_basis_in heterozygous mutation in the THSD1 gene on chromosome 13q14. |
13 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0060228 | DOID:0080975 |
| is_a | DOID:10941 | DOID:0080975 |
| is_a | DOID:6713 | DOID:0080975 |
| is_a | DOID:0050828 | DOID:0080975 |
| is_a | DOID:3527 | DOID:0080975 |
| is_a | DOID:936 | DOID:0080975 |
| is_a | DOID:4 | DOID:0080975 |
| is_a | DOID:13089 | DOID:0080975 |
| is_a | DOID:863 | DOID:0080975 |
| is_a | DOID:178 | DOID:0080975 |
| is_a | DOID:331 | DOID:0080975 |
| is_a | DOID:7 | DOID:0080975 |
| is_a | DOID:1287 | DOID:0080975 |
