Myoclonus and ataxia

Preferred Label : Myoclonus and ataxia;

Obsolete resource : true;

Moved to : 213400;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Ramsay hunt syndrome;

Inheritance : Autosomal dominant; heterogeneous;

Prefixed ID : 159700;

Details

Origin ID

159700;

UMLS CUI

C1834580;

Automatic exact mappings (from CISMeF team)
- Early onset cerebellar ataxia with myoclonus (disorder) [SNOMED CT concept]
- Geniculate ganglionitis [ICD-11 More detail]
- Ramsay Hunt syndrome [PASCAL descriptor]
- myoclonic cerebellar dyssynergia [MeSH Descriptor]
Currated CISMeF NLP mapping
- Hunt's syndrome [MeSH concept]
- Ramsay Hunt syndrome [ORDO Disease]
- Ramsay-Hunt syndrome [MedDRA LLT]
- hunt's syndrome [MeSH Supplementary Concept]
False automatic mappings
- herpes zoster oticus [Disease (Nov.)]
- herpes zoster oticus [MeSH Descriptor]
- herpes zoster oticus [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hunt's syndrome [MeSH concept]
- hunt's syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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