1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0070456 | hereditary spastic paraplegia 87 | A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM63C gene on chromosome 14q24.3. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| 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. |
