1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0070445 | early-onset dystonia and/or spastic paraplegia | A dystonia characterized by variable onset of dystonia, spasticity, or both that has_material_basis_in heterozygous mutation in the ATP5MC3 gene on chromosome 2q31.1. |
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. |