Search Ontology:
Human Disease

leukoencephalopathy with vanishing white matter 5

Term ID
DOID:0070367
Synonyms
Definition
A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B5 gene on chromosome 3q27. (3)
References
Ontology
Human Disease   ( DOID:0070367 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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