Optic Atrophy, Autosomal Dominant
Information
- Disease name
- Optic Atrophy, Autosomal Dominant
- Disease ID
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT06140329 | Recruiting | Natural History of Autosomal Dominant Optic Atrophy (ADOA), Caused by OPA1 Mutation | February 28, 2024 | June 2026 | |
| NCT01522638 | Unknown status | Advanced Characterization of Autosomal Dominant Optic Atrophy | December 2011 | June 2015 |
- MeSH unique ID (MeSH (Medical Subject Headings))
- D029241