1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0080285 | developmental and epileptic encephalopathy 58 | A developmental and epileptic encephalopathy characterized by onset in the first days or months of life of infantile spasms and refractory seizures, global developmental delay, and impaired intellectual development that has_material_basis_in heterozygous mutation in the NTRK2 gene on chromosome 9q21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| 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. |
