ophthalmoplegia
Information
- Disease name
- ophthalmoplegia
- Disease ID
- DOID:539
- 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 |
|---|---|---|---|---|---|
| NCT03135574 | Completed | Prevalence of a High-intensity Signal of the Oculomotor Nerve on T2 MRI Sequence in Patients With Ophthalmoplegia | April 16, 2017 | February 22, 2021 | |
| NCT03269682 | Completed | Prevalence of Contrast Enhancement of the Oculomotor Nerve on 3D PD T1 MRI Sequence in Patients With Ophthalmoplegia | October 20, 2017 | April 16, 2021 | |
| NCT04436198 | Terminated | N/A | Capsular Tension Rings in Intraocular Lens Rotation | September 1, 2020 | April 21, 2023 |
- Disase is a (Disease Ontology)
- DOID:1279
- Cross Reference ID (Disease Ontology)
- ICD9CM:378.56
- Cross Reference ID (Disease Ontology)
- MESH:D009886
- Cross Reference ID (Disease Ontology)
- NCI:C79697
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:16110005
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:78097002
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0029089
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0155338
- Exact Synonym (Disease Ontology)
- extraocular muscle paralysis
- Exact Synonym (Disease Ontology)
- eye movement paralysis
- Exact Synonym (Disease Ontology)
- oculomotor paralysis
- Exact Synonym (Disease Ontology)
- Total ophthalmoplegia
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0000602
- MeSH unique ID (MeSH (Medical Subject Headings))
- D009886