8 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: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:10579 | leukodystrophy | A cerebral degeneration characterized by dysfunction of the white matter of the brain. |
DOID:1443 | cerebral degeneration | A brain disease that is characterized by loss of structure or function of neurons, including death of neurons and loss of brain tissue. |
DOID:13945 | CADASIL | A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment. |
9 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:13945 | DOID:0111035 |
is_a | DOID:13945 | DOID:0111036 |
is_a | DOID:10579 | DOID:13945 |
is_a | DOID:331 | DOID:13945 |
is_a | DOID:863 | DOID:13945 |
is_a | DOID:1443 | DOID:13945 |
is_a | DOID:7 | DOID:13945 |
is_a | DOID:4 | DOID:13945 |
is_a | DOID:936 | DOID:13945 |