Leukoencephalopathy with vanishing white matter 2

Preferred Label : Leukoencephalopathy with vanishing white matter 2;

Symbol : VWM2;

Type : Phenotype, molecular basis known;

Prefixed ID : #620312;

Details

Origin ID

620312;

UMLS CUI

C5830404;

Genes related to phenotype
- Eukaryotic translation initiation factor 2b, subunit 2 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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