7 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:0111297 | familial febrile seizures | A brain disease characterized by seizures during childhood associated with febrile episodes without any evidence of intracranial infection or defined pathologic or traumatic cause with a familial pattern of inheritance. |
| DOID:0111311 | familial febrile seizures 7 | A familial febrile seizures that has_material_basis_in heterozygous mutation. |
6 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0111297 | DOID:0111311 |
| is_a | DOID:331 | DOID:0111311 |
| is_a | DOID:7 | DOID:0111311 |
| is_a | DOID:863 | DOID:0111311 |
| is_a | DOID:4 | DOID:0111311 |
| is_a | DOID:936 | DOID:0111311 |
