All diseases

OMIM ID
603896
OMIM term:
LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM
Alternative terms:
CHILDHOOD ATAXIA WITH CENTRAL NERVOUS SYSTEM HYPOMYELINIZATION; CACH
VANISHING WHITE MATTER LEUKODYSTROPHY
CREE LEUKOENCEPHALOPATHY; CLE VANISHING WHITE MATTER LEUKODYSTROPHY WITH OVARIAN FAILURE, INCLUDED
OVARIOLEUKODYSTROPHY, INCLUDED
(∗) Location:
12q24.31   14q24.3   1p34.1   2p23.3   3q27.1  
(†) Associated OMIM genes:
EIF2B1   EIF2B2   EIF2B3   EIF2B4   EIF2B5  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/2buml2i1