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DO Term : leukoencephalopathy with vanishing white matter 3 [DOID:0070372] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B3 gene on chromosome 1p34.

synonyms:
620313,
OMIM:620313

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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