Leukoencephalopathy with Vanishing White Matter 4 (VWM4)

Alias:
Leukoencephalopathy with Vanishing White Matter 4, with or Without Ovarian Failure
Vwm4
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Leukoencephalopathy with Vanishing White Matter 4, also known as vwm4, is related to leukoencephalopathy with vanishing white matter and leukoencephalopathy with vanishing white matter 1. An important gene associated with Leukoencephalopathy with Vanishing White Matter 4 is EIF2B4 (Eukaryotic Translation Initiation Factor 2B Subunit Delta). Affiliated tissues include brain, and related phenotypes are spasticity and optic atrophy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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1
5
3

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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