Any dystonic disorder in which the cause of the disease is a mutation in the KMT2B gene.
Comprehensive, easy-to-understand information about this condition
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lymphatic malformation 5
MONDO:0007920
Woodhouse-Sakati syndrome
MONDO:0009419
severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
MONDO:0010334
torsion dystonia 7
MONDO:0011200
developmental malformations-deafness-dystonia syndrome
MONDO:0011823
dopa-responsive dystonia due to sepiapterin reductase deficiency
MONDO:0012994