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Human Disease and Mouse Model Detail
Human Disease

Term: Leukoencephalopathy with Vanishing White Matter; VWM
OMIM ID: 603896

Synonyms Childhood Ataxia with Central Nervous System Hypomyelinization; CACH; Vanishing White Matter Leukodystrophy
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Eif2b1 EIF2B1
Eif2b2 EIF2B2
Eif2b3 EIF2B3
Eif2b4 EIF2B4
Eif2b5 EIF2B5
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory