9 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:10024 | migraine with aura | A migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon. |
| DOID:0060178 | familial hemiplegic migraine | A migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body (hemiparesis). Additional features of an aura can include difficulty with speech, confusion, and drowsiness. |
| DOID:6364 | migraine | A brain disease that is characterized by moderate to severe headaches, nausea, extreme sensitivity to light and sound and intense unilaterial throbbing or pulsing. |
| DOID:0111183 | familial hemiplegic migraine 3 | A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in SCN1A on 2q24.3. |
8 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0060178 | DOID:0111183 |
| is_a | DOID:6364 | DOID:0111183 |
| is_a | DOID:863 | DOID:0111183 |
| is_a | DOID:4 | DOID:0111183 |
| is_a | DOID:10024 | DOID:0111183 |
| is_a | DOID:936 | DOID:0111183 |
| is_a | DOID:331 | DOID:0111183 |
| is_a | DOID:7 | DOID:0111183 |
