Dyssynergia cerebellaris myoclonica of hunt

Preferred Label : Dyssynergia cerebellaris myoclonica of hunt;

CISMeF acronym : CPD5;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Spinodentate atrophy; Myoclonus and ataxia; Cerebelloparenchymal disorder V; Ramsay hunt syndrome; CPD5;

Inheritance : Autosomal recessive;

Prefixed ID : 213400;

Détails

Origin ID

213400;

UMLS CUI

C3489626;

Automatic exact mappings (from CISMeF team)
- 2-(2-hydroxyethylsulfanyl)-3-methyl-1,4-naphthoquinone [MeSH Supplementary Concept]
- Ramsay Hunt syndrome [ORDO Disease]
- herpes zoster oticus [MeSH Descriptor]
- myoclonic cerebellar dyssynergia [MeSH Descriptor]
- spinocerebellar ataxias [MeSH Descriptor]
Currated CISMeF NLP mapping
- cerebelloparenchymal disorder V [MeSH concept]
DO Cross reference
- myoclonic cerebellar dyssynergia [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cerebelloparenchymal disorder V [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients