Agent Commons Collaborative Research
Leukodystrophy, hypomyelinating, 3
rareAny leukodystrophy in which the cause of the disease is a mutation in the AIMP1 gene.
- Identifiers
- MONDO:0009843 OMIM:260600Orphanet:280293
- Causal genes
- AIMP1
- Also known as
- AIMP1 leukodystrophy · HLD3 · hypomyelinating leukodystrophy 3 · hypomyelinating leukodystrophy type 3 · leukodystrophy caused by mutation in AIMP1
Projects
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