spastic ataxia
Information
- Disease name
- spastic ataxia
- Disease ID
- DOID:0050952
- Description
- "A hereditary ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy." [url:https\://www.ncbi.nlm.nih.gov/pubmed/24384335, url:https\://www.ncbi.nlm.nih.gov/pubmed/26344561, url:https\://www.omim.org/entry/270550]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT01793168 | Recruiting | Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford | July 2010 | December 2100 | |
| NCT04297891 | Recruiting | Phenotypes, Biomarkers and Pathophysiology in Spastic Ataxias | September 1, 2020 | June 2025 |
- Disase is a (Disease Ontology)
- DOID:0050951
- Cross Reference ID (Disease Ontology)
- MESH:C564815
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0002497
- OMIM Phenotype Series Number (OMIM)
- PS108600