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Human Disease and Mouse Model Detail
Human Disease Leukoencephalopathy with Vanishing White Matter; VWM
OMIM ID: 603896
Human Phenotype Ontology associations
Synonyms Childhood Ataxia with Central Nervous System Hypomyelinization; CACH; Vanishing White Matter Leukodystrophy
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     EIF2B5* Eif2b5* View 2 models HomoloGene and HGNC
     EIF2B1* Eif2b1   HomoloGene and HGNC
EIF2B2* Eif2b2   HomoloGene and HGNC
EIF2B3* Eif2b3   HomoloGene and HGNC
EIF2B4* Eif2b4   HomoloGene and HGNC
References Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory