Unverricht-Lundborg syndrome

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Information
Disease name
Unverricht-Lundborg syndrome
Disease ID
DOID:3535
Description
"A progressive myoclonus epilepsy characterized by onset between 6 and 13 years of age of action- and stimulus-sensitive myoclonus, tonic-clonic seizures with ataxia, and a mild cognitive decline." [url:https\://www.ncbi.nlm.nih.gov/pubmed/19469843]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT00639119 Unknown status Phase 2 Effect of Ropinirole Hydrochloride in Progressive Myoclonic Epilepsy of Unverricht-Lundborg Type August 2007
Disase is a (Disease Ontology)
DOID:891
Cross Reference ID (Disease Ontology)
GARD:3876
Cross Reference ID (Disease Ontology)
MESH:D020194
Cross Reference ID (Disease Ontology)
NCI:C179710
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:192847001
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0751785
Exact Synonym (Disease Ontology)
Unverricht - Lundborg disease
Exact Synonym (Disease Ontology)
Unverricht's disease
Exact Synonym (Disease Ontology)
Unverricht-Lundborg disease
MedGen concept unique identifier (MedGen Concept name)
C0751785
MedGen unique identifier (MedGen Concept name)
155923
MeSH unique ID (MeSH (Medical Subject Headings))
D020194