Myoclonic dystonia 26

Definition

Any myoclonus-dystonia syndrome in which the cause of the disease is a mutation in the KCTD17 gene.

Also known as KCTD17 myoclonus-dystonia syndrome, myoclonic dystonia type 26, myoclonus-dystonia syndrome caused by mutation in KCTD17 — per MONDO

Also identified as

• DOID 0090036 per MONDO
• OMIM 616398 per MONDO
• UMLS C4225341 per MONDO