Agent Commons Collaborative Research
Dystonia 28, childhood-onset
rareAny dystonic disorder in which the cause of the disease is a mutation in the KMT2B gene.
- Identifiers
- MONDO:0015004 OMIM:617284Orphanet:589618
- Causal genes
- KMT2B
- Part of
- Inherited dystonia
- Also known as
- dystonia 28, childhood-onset; DYT28 · dystonic disorder caused by mutation in KMT2B · DYT28 · KMT2B dystonic disorder
Projects
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