Spinocerebellar ataxia type 38 (disorder) | | Spinocerebellar ataxia type 38 | | Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplopia and axonal neuropathy. | | spinocerebellaire ataxie type 38 | | SCA38
|
| Id | 734021001 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | G11.8 | Rule | TRUE | Advice | ALWAYS G11.8 | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|