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| Term | leukoencephalopathy with vanishing white matter 1 | ID (Ontology) | DOID:0070374 (Human Disease) |
| Definition | A leukoencephalopathy with vanishing white matter that has_material_basis_in homozygous or compound heterozygous mutation in the EIF2B1 gene on chromosome 12q24. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal recessive disease__ leukodystrophy_______________| leukoencephalopathy with vanishing white matter |__leukoencephalopathy with vanishing white matter 1 1 rec. |
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| Is a | leukoencephalopathy with vanishing white matter | ||
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| MIM:603896 | |||