12 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:2914 | immune system disease | A disease of anatomical entity that is located_in the immune system. |
DOID:417 | autoimmune disease | An immune system disease that is an overactive immune response of the body against substances and tissues normally present in the body resulting from an abnormal functioning of the immune system that results in the production of antibodies or T cell directed against the host tissues. |
DOID:438 | autoimmune disease of the nervous system | An autoimmune disease affecting the nervous system. |
DOID:612 | primary immunodeficiency disease | An immune system disease that results when one or more essential parts of the immune system is missing or not working properly at birth due to a genetic mutation. |
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:1826 | epilepsy | A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions. |
DOID:0060004 | autoimmune disease of central nervous system | An autoimmune hypersensitivity disease located_in the central nervous system. |
DOID:0080994 | autoimmune epilepsy | An epilepsy that is characterized by new-onset refractory seizures along with subacute progressive cognitive decline and behavioral or psychiatric dysfunction. |
11 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:0060004 | DOID:0080994 |
is_a | DOID:1826 | DOID:0080994 |
is_a | DOID:331 | DOID:0080994 |
is_a | DOID:936 | DOID:0080994 |
is_a | DOID:2914 | DOID:0080994 |
is_a | DOID:438 | DOID:0080994 |
is_a | DOID:7 | DOID:0080994 |
is_a | DOID:417 | DOID:0080994 |
is_a | DOID:4 | DOID:0080994 |
is_a | DOID:863 | DOID:0080994 |
is_a | DOID:612 | DOID:0080994 |