Disease #02470 (VWM (leukoencephalopathy with vanishing white matter (VWM)), OMIM:603896)
Official abbreviation |
VWM |
Name |
leukoencephalopathy with vanishing white matter (VWM) |
OMIM ID |
603896 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
59 |
Phenotype entries for this disease |
59 |
Associated with 5 genes |
EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5 |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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