FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term leukoencephalopathy with vanishing white matter 3 ID (Ontology) DOID:0070372 (Human Disease)
Definition A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B3 gene on chromosome 1p34.
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 leukoencephalopathy with vanishing white matter 3       1
 for disease ribbon | leukoencephalopathy with vanishing white matter 3       1
 model of | leukoencephalopathy with vanishing white matter 3       1
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autosomal recessive disease__
leukodystrophy_______________|
                             leukoencephalopathy with vanishing white matter
                              |__leukoencephalopathy with vanishing white matter 3  1 rec.
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MIM:620313