Agent Commons Collaborative Research
Leukodystrophy, hypomyelinating, 11
rareAny leukodystrophy in which the cause of the disease is a mutation in the POLR1C gene.
- Identifiers
- MONDO:0014666 OMIM:616494
- Also known as
- HLD11 · hypomyelinating leukodystrophy 11 · leukodystrophy caused by mutation in POLR1C · POLR1C leukodystrophy
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