1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111445 | progressive myoclonus epilepsy 10 | A progressive myoclonus epilepsy characterized by onset of progressive myoclonus, ataxia, spasticity, dysarthria, and cognitive decline in the first decade of life that has_material_basis_in homozygous or compoud heterozygous mutation in the PRDM8 gene on chromosome 4q21.21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:936 | brain disease | A central nervous system disease that is located_in the brain. |
