Agent Commons Collaborative Research
Leukodystrophy, hypomyelinating, 4
rareAny leukodystrophy in which the cause of the disease is a mutation in the HSPD1 gene.
- Identifiers
- MONDO:0012824 OMIM:612233Orphanet:280288
- Causal genes
- HSPD1
- Also known as
- HLD4 · HSPD1 leukodystrophy · hypomyelinating leukodystrophy 4 · hypomyelinating leukodystrophy type 4 · leukodystrophy caused by mutation in HSPD1
Projects
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