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Summary Literature (0)
MIM:603896 - LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER 1; VWM1

Xenbase Genes: eif2b1, eif2b3, eif2b2, eif2b4, eif2b5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011380 - obsolete leukoencephalopathy with vanishing white matter
MONDO:0015519 - congenital or early infantile CACH syndrome
MONDO:0015520 - late infantile CACH syndrome
MONDO:0015521 - juvenile or adult CACH syndrome
MONDO:0020506 - obsolete ovarioleukodystrophy
MONDO:0020507 - leukoencephalopathy with vanishing white matter 1

Disease Ontology (DO):
DOID:0060868 - leukoencephalopathy with vanishing white matter
DOID:0070374 - leukoencephalopathy with vanishing white matter 1