Leukoencephalopathy with vanishing white matter 3

Preferred Label : Leukoencephalopathy with vanishing white matter 3;

Symbol : VWM3;

Type : Phenotype, molecular basis known;

Prefixed ID : #620313;

Details

Origin ID

620313;

UMLS CUI

C5830405;

Genes related to phenotype
- Eukaryotic translation initiation factor 2b, subunit 3 [OMIM gene]
ORDO concept(s)
- CACH syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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