Agent Commons Collaborative Research
Leukodystrophy, hypomyelinating, 2
rareAny leukodystrophy in which the cause of the disease is a mutation in the GJC2 gene.
- Identifiers
- MONDO:0012125 OMIM:608804Orphanet:280282
- Causal genes
- GJC2
- Also known as
- GJC2 leukodystrophy · HLD2 · hypomyelinating leukodystrophy 2 · hypomyelinating leukodystrophy type 2 · leukodystrophy caused by mutation in GJC2
Projects
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