Macular dystrophy
Information
- Disease name
- Macular dystrophy
- 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 |
|---|---|---|---|---|---|
| NCT05927740 | Completed | N/A | The Efficacy of Hyperemesis Gravidarum on Macular Thickness, Corneal Thickness and Intraocular Pressure in Pregnancy | March 10, 2020 | May 11, 2023 |
| NCT02255981 | Completed | N/A | Efficacy of Acupuncture in Macular Diseases | March 2013 | November 2016 |
| NCT04620876 | Recruiting | N/A | Bimodal and Coaxial High Resolution Ophtalmic Imaging | October 1, 2019 | October 15, 2024 |
| NCT05793515 | Recruiting | Mechanisms of Inherited Retinal Dystrophies Using Whole Genome Sequencing and in Vitro and in Vivo Models | November 15, 2022 | November 15, 2025 | |
| NCT04129021 | Unknown status | N/A | Multimodal Ophthalmic Imaging | July 15, 2019 | June 30, 2023 |
| NCT04128150 | Unknown status | High Resolution Retina Imaging | January 17, 2018 | January 30, 2024 | |
| NCT01278277 | Unknown status | Phase 1/Phase 2 | Saffron Supplementation in Stargardt's Disease | February 2011 | December 2017 |
- HPO alt_id (Human Phenotype Ontology)
- HP:0007638
- HPO alt_id (Human Phenotype Ontology)
- HP:0007798
- HPO alt_id (Human Phenotype Ontology)
- HP:0007914
- HPO alt_id (Human Phenotype Ontology)
- HP:0007919
- HPO alt_id (Human Phenotype Ontology)
- HP:0007999
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0007754
- MedGen concept unique identifier (MedGen Concept name)
- C0730292
- MedGen unique identifier (MedGen Concept name)
- 196451