Albinism, Ocular
Information
- Disease name
- Albinism, Ocular
- 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 |
|---|---|---|---|---|---|
| NCT00001153 | Completed | Visual Function and Ocular Pigmentation in Albinism | June 1976 | May 2000 | |
| NCT03959605 | Completed | Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children | January 6, 2019 | October 1, 2021 | |
| NCT06345976 | Not yet recruiting | Functional Impairment in Albinism | May 2024 | May 2025 | |
| NCT04495218 | Recruiting | NGS Panel of Incomplete Forms of Ocular Albinism | November 23, 2020 | June 2024 |
- MeSH unique ID (MeSH (Medical Subject Headings))
- D016117