alternating hemiplegia of childhood
Information
- Disease name
- alternating hemiplegia of childhood
- Disease ID
- DOID:0050635
- Description
- "A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body." [url:http\://en.wikipedia.org/wiki/Alternating_hemiplegia_of_childhood, url:http\://ghr.nlm.nih.gov/condition/alternating-hemiplegia-of-childhood]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes | Mutation | Description | Source | Links |
---|
NCT ID | Status | Phase | Summary | Start date | Completion date |
---|---|---|---|---|---|
NCT00931164 | Completed | Phase 1/Phase 2 | Sodium Oxybate in Patients With Alternating Hemiplegia of Childhood (AHC-SO) | August 2009 | September 2011 |
NCT02408354 | Completed | Phase 2 | Pilot Study, Comparative, Single-center, Randomized, Crossover, Double-blind, Against Placebo, Testing the Effectiveness of Triheptanoin Oil in Alternating Hemiplegia of Childhood | April 15, 2015 | April 5, 2017 |
NCT04944927 | Completed | HEmiplegia Arrhythmia Retrospective Trial | April 29, 2021 | June 29, 2022 | |
NCT06248645 | Not yet recruiting | Phase 2 | Oxygen as an Acute Treatment in Alternating Hemiplegia of Childhood | April 2024 | March 2025 |
NCT03857607 | Unknown status | Natural History Study of ATP1A3-related Disease | September 1, 2018 | August 31, 2023 |
- Disase is a (Disease Ontology)
- DOID:10969
- Cross Reference ID (Disease Ontology)
- GARD:11
- Cross Reference ID (Disease Ontology)
- ICD10CM:G98
- Cross Reference ID (Disease Ontology)
- MESH:C536589
- Cross Reference ID (Disease Ontology)
- MIM:104290
- Cross Reference ID (Disease Ontology)
- MIM:614820
- Cross Reference ID (Disease Ontology)
- MIM:PS104290
- Cross Reference ID (Disease Ontology)
- ORDO:2131
- Exact Synonym (Disease Ontology)
- AHC
- OMIM Phenotype Series Number (OMIM)
- PS104290
- OrphaNumber from OrphaNet (Orphanet)
- 2131
- MedGen concept unique identifier (MedGen Concept name)
- C0338488
- MedGen unique identifier (MedGen Concept name)
- 90925