Encephalitis/encephalopathy, mild, with reversible myelin vacuolization

Preferred Label : Encephalitis/encephalopathy, mild, with reversible myelin vacuolization;

Symbol : MMERV;

CISMeF acronym : MERS; MMERV;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Encephalitis/encephalopathy, mild, with reversible splenial lesion; MERS;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the myelin regulatory factor gene (MYRF, 608329.0001);

Prefixed ID : #618113;

Détails

Origin ID

618113;

UMLS CUI

C4722446;

Automatic exact mappings (from CISMeF team)
- Coastal environment (environment) [SNOMED CT concept]
- MERS [MedDRA LLT]
- Middle East Respiratory Syndrome [NCIt concept]
- Middle East respiratory syndrome [ORDO Disease]
- Middle East respiratory syndrome [COVID-19 Thesaurus concept]
- covid-19 (coronavirus disease 2019) [MedlinePlus Topic]
- mercury (II) reductase activity [GO term]
- oceans and seas [MeSH Descriptor]
- seas [MeSH concept]
Genes related to phenotype
- Myelin regulatory factor [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Delayed speech and language development [HPO term]
- Seizure [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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

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