1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0050981 | spinocerebellar ataxia type 34 | An autosomal dominant cerebellar ataxia that is characterized by papulosquamous, ichthyosiform plaques at birth and progressive ataxia, dysarthria, nystagmus and hyporeflexia, has_material_basis_in mutation in the ELOVL4 gene. |
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. |
