olivopontocerebellar atrophy
GPTKB entity
Statements (28)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
neurodegenerative disease
|
| gptkbp:affects |
gptkb:cerebellum
pons inferior olivary nucleus |
| gptkbp:cause |
genetic disorder
|
| gptkbp:diagnosedBy |
neurological examination
MRI |
| gptkbp:firstDescribed |
early 20th century
|
| https://www.w3.org/2000/01/rdf-schema#label |
olivopontocerebellar atrophy
|
| gptkbp:ICD-10_code |
G11.1
|
| gptkbp:prevalence |
rare
|
| gptkbp:progression |
progressive
|
| gptkbp:relatedTo |
gptkb:Friedreich's_ataxia
gptkb:multiple_system_atrophy |
| gptkbp:subspecies |
spinocerebellar ataxia
hereditary olivopontocerebellar atrophy sporadic olivopontocerebellar atrophy |
| gptkbp:symptom |
tremor
ataxia dysphagia muscle rigidity dysarthria |
| gptkbp:treatment |
occupational therapy
physical therapy speech therapy |
| gptkbp:bfsParent |
gptkb:Multiple_System_Atrophy
gptkb:multiple_system_atrophy |
| gptkbp:bfsLayer |
7
|