All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02470 VWM leukoencephalopathy with vanishing white matter (VWM) 603896 AR 58 58 EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 - autosomal recessive
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