hereditary ataxia
Information
- Disease name
- hereditary ataxia
- Disease ID
- DOID:0050951
- Description
- "A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements." [url:http\://www.ncbi.nlm.nih.gov/books/NBK1138]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT06152133 | Active, not recruiting | N/A | Telerehabilitation, Core Stability Exercises and Hereditary Ataxia (TRCore-ataxia) | March 1, 2024 | December 1, 2025 |
| NCT00202397 | Completed | Phase 2 | Effect of Riluzole as a Symptomatic Approach in Patients With Chronic Cerebellar Ataxia | June 2005 | August 2008 |
| NCT00004306 | Completed | Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10) | November 1999 | March 2009 | |
| NCT04750850 | Completed | N/A | Core Stability Exercises and Hereditary Ataxia | May 20, 2021 | January 10, 2023 |
| NCT05160870 | Recruiting | Genotype-phenotype Correlation and Pathogenic Mechanism in Hereditary Ataxia | June 30, 2021 | December 25, 2025 | |
| NCT05160883 | Recruiting | Neuroimaging Changes in Hereditary Ataxia | June 30, 2021 | December 25, 2025 | |
| NCT01360164 | Unknown status | Phase 1/Phase 2 | Safety and Efficacy of Umbilical Cord Mesenchymal Stem Cell Therapy for Patients With Hereditary Ataxia | January 2010 | December 2013 |
- Disase is a (Disease Ontology)
- DOID:1289
- Cross Reference ID (Disease Ontology)
- GARD:6614
- ICD10 preferred id (Insert disease from ICD10)
- D0005262
- ICD10 class code (Insert disease from ICD10)
- G11