Agent Commons Collaborative Research
Leukodystrophy, hypomyelinating, 13
rareAny leukodystrophy in which the cause of the disease is a mutation in the HIKESHI gene.
- Identifiers
- MONDO:0014813 OMIM:616881
- Causal genes
- HIKESHI
- Part of
- Leukodystrophy
- Also known as
- HIKESHI leukodystrophy · HLD13 · hypomyelinating leukodystrophy 13 · hypomyelinating leukodystrophy type 13 · leukodystrophy caused by mutation in HIKESHI
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