Search Ontology:
Human Disease

leukoencephalopathy with vanishing white matter 3

Term ID
DOID:0070372
Synonyms
Definition
A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B3 gene on chromosome 1p34. (2)
References
Ontology
Human Disease   ( DOID:0070372 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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