retinitis
Information
- Disease name
- retinitis
- Disease ID
- DOID:3612
- 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 |
---|---|---|---|---|---|
NCT04123626 | Active, not recruiting | Phase 1/Phase 2 | A Study to Evaluate the Safety and Tolerability of QR-1123 in Subjects With Autosomal Dominant Retinitis Pigmentosa Due to the P23H Mutation in the RHO Gene | October 7, 2019 | June 7, 2022 |
NCT00001734 | Completed | Screening for NEI Clinical Studies | March 23, 1998 | October 3, 2008 | |
NCT03753893 | Completed | Ocular Manifestations in Rheumatic Diseases | May 1, 2013 | November 1, 2021 | |
NCT04945772 | Completed | Phase 2 | Efficacy and Safety of MCO-010 Optogenetic Therapy in Adults With Retinitis Pigmentosa [RESTORE] | July 13, 2021 | January 18, 2024 |
NCT06162585 | Enrolling by invitation | Non-Interventional Long Term Follow-up Study of Participants Previously Enrolled in the RESTORE Study | December 8, 2023 | September 2027 | |
NCT00550498 | Terminated | Phase 1 | Stem Cell Transplantation in Ocular Lesions of Behcet's Disease | December 2007 | July 2013 |
- Disase is a (Disease Ontology)
- DOID:5679
- Cross Reference ID (Disease Ontology)
- ICD10CM:H30.9
- Cross Reference ID (Disease Ontology)
- MESH:D012173
- Cross Reference ID (Disease Ontology)
- NCI:C115993
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:35426003
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0035333
- MedGen concept unique identifier (MedGen Concept name)
- C0035333
- MedGen unique identifier (MedGen Concept name)
- 19765
- MeSH unique ID (MeSH (Medical Subject Headings))
- D012173