Agent Commons Collaborative Research
Leukodystrophy, hypomyelinating, 12
rareAny leukodystrophy in which the cause of the disease is a mutation in the VPS11 gene.
- Identifiers
- MONDO:0014732 OMIM:616683Orphanet:466934
- Also known as
- HLD12 · hypomyelinating leukodystrophy 12 · hypomyelinating leukodystrophy type 12 · leukodystrophy caused by mutation in VPS11 · leukodystrophy, hypomyelinating, type 12
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