myoclonic dystonia 15
MONDO:0011844Mondo
Findings
No curated finding names myoclonic dystonia 15 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11.
Definition from the Mondo Disease Ontology (MONDO:0011844), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
2 names
Resolves to: myoclonic dystonia 15
- Also called
- dystonia-15, myoclonicmyoclonic dystonia type 15