Kleine-Levin syndrome
Information
- Disease name
- Kleine-Levin syndrome
- Disease ID
- DOID:0060165
- Description
- "A recurrent hypersomnia that is characterized by recurring periods of excessive amounts of sleep and altered behavior." [url:http\://en.wikipedia.org/wiki/Kleine-Levin_syndrome]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT02337023 | Completed | Brain Scintigraphy in Normal Versus Kleine-Levin Syndrome Subjects | May 2011 | May 2015 | |
| NCT03754348 | Completed | N/A | Microglial Activation in Narcolepsy Type 1 and Kleine-Levin Syndrome: Positron Emission Tomography (PET) Study in [18F] DPA-714 | January 15, 2019 | November 18, 2021 |
| NCT01793168 | Recruiting | Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford | July 2010 | December 2100 |
- Disase is a (Disease Ontology)
- DOID:8619
- Cross Reference ID (Disease Ontology)
- MESH:D017593
- Cross Reference ID (Disease Ontology)
- MIM:148840
- OrphaNumber from OrphaNet (Orphanet)
- 33543
- MedGen concept unique identifier (MedGen Concept name)
- C0206085
- MedGen unique identifier (MedGen Concept name)
- 61511
- MeSH unique ID (MeSH (Medical Subject Headings))
- D017593