Congenital blindness
Information
- Disease name
- Congenital blindness
- 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 |
|---|---|---|---|---|---|
| NCT03968991 | Terminated | N/A | VISIODOL: Validation of the VISIODOL® Scale | June 18, 2019 | December 28, 2020 |
- HPO alt_id (Human Phenotype Ontology)
- HP:0007706
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0007875