alternating hemiplegia of childhood

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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