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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Inherited neurodegenerative disorder
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Leukodystrophy
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Leukoencephalopathy with vanishing white matter
Leukoencephalopathy with vanishing white matter 5
rare
Identifiers
MONDO:0957873
OMIM:620315
Causal genes
EIF2B5
Part of
Leukoencephalopathy with vanishing white matter
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