Leukoencephalopathy with vanishing white matter 5

Preferred Label : Leukoencephalopathy with vanishing white matter 5;

Symbol : VWM5;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Cree leukoencephalopathy; CLE;

Prefixed ID : #620315;

Détails

Origin ID

620315;

UMLS CUI

C5779973;

Currated CISMeF NLP mapping
- Cree leukoencephalopathy [ORDO Disease]
- Cree leukoencephalopathy [ICD-11 More detail]
Genes related to phenotype
- Eukaryotic translation initiation factor 2b, subunit 5 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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