Log In|Sign Up
ENLeukoencephalopathy with Vanishing White Matter 2 (VWM2)
Alias:
Leukoencephalopathy with Vanishing White Matter 2, with or Without Ovarian Failure
Vwm2
Favorite
Leukoencephalopathy with Vanishing White Matter 2, is also known as vwm2. An important gene associated with Leukoencephalopathy with Vanishing White Matter 2 is EIF2B2 (Eukaryotic Translation Initiation Factor 2B Subunit Beta). Affiliated tissues include brain and cortex, and related phenotypes are spasticity and cataract
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
