18 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:0050177 | monogenic disease | A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:0050736 | autosomal dominant disease | An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease. |
| DOID:0050739 | autosomal genetic disease | A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. |
| 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:0080966 | intracranial berry aneurysm 3 | 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 has been mapped to chromosome 1p36. |
17 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050736 | DOID:0080966 |
| is_a | DOID:0060228 | DOID:0080966 |
| is_a | DOID:936 | DOID:0080966 |
| is_a | DOID:7 | DOID:0080966 |
| is_a | DOID:0050177 | DOID:0080966 |
| is_a | DOID:13089 | DOID:0080966 |
| is_a | DOID:1287 | DOID:0080966 |
| is_a | DOID:0050739 | DOID:0080966 |
| is_a | DOID:0050828 | DOID:0080966 |
| is_a | DOID:6713 | DOID:0080966 |
| is_a | DOID:630 | DOID:0080966 |
| is_a | DOID:3527 | DOID:0080966 |
| is_a | DOID:863 | DOID:0080966 |
| is_a | DOID:10941 | DOID:0080966 |
| is_a | DOID:4 | DOID:0080966 |
| is_a | DOID:178 | DOID:0080966 |
| is_a | DOID:331 | DOID:0080966 |
