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: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:2476 | hereditary spastic paraplegia | A paraplegia that is characterized by progressive stiffness and contraction (spasticity) in the lower limbs. |
| DOID:607 | paraplegia | |
| DOID:0060245 | Mast syndrome | A hereditary spastic paraplegia associated with dementia. |
6 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:2476 | DOID:0060245 |
| is_a | DOID:4 | DOID:0060245 |
| is_a | DOID:607 | DOID:0060245 |
| is_a | DOID:331 | DOID:0060245 |
| is_a | DOID:7 | DOID:0060245 |
| is_a | DOID:863 | DOID:0060245 |
