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:480 | movement disease | A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity. |
| DOID:4990 | essential tremor | A movement disorder that causes involuntary tremors, especially in the hands. It occurs alone without other neurological signs and symptoms. |
| DOID:0111430 | essential tremor 3 | An essential tremor that has_material_basis_in variation in a region on chromosome 6p23. |
7 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:4990 | DOID:0111430 |
| is_a | DOID:331 | DOID:0111430 |
| is_a | DOID:863 | DOID:0111430 |
| is_a | DOID:4 | DOID:0111430 |
| is_a | DOID:7 | DOID:0111430 |
| is_a | DOID:480 | DOID:0111430 |
| is_a | DOID:936 | DOID:0111430 |
