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Dystonia 28, childhood-onset

MONDO:0015004

Any dystonic disorder in which the cause of the disease is a mutation in the KMT2B gene.

Also known as: DYT28, KMT2B dystonic disorder, dystonia 28, childhood-onset, dystonia 28, childhood-onset; DYT28, dystonic disorder caused by mutation in KMT2B

14 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Movement disorder (89) Dystonic disorder (60) Human disease (14) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 10 Not yet finished but already full! 1 Completed 3
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