Dystonia 5

MONDO:0007495

An autosomal dominant dopa-responsive dystonia in which the cause of the disease is a variation in the GCH1 gene.

Also known as: DYT-GCH1, Dopa-responsive dystonia, autosomal dominant, GTP cyclohydrolase 1-deficient dopa-responsive dystonia, Segawa Syndrome, Segawa syndrome, autosomal dominant, dystonia 5, dystonia type 5, dystonia, DOPA-responsive, with or without hyperphenylalaninemia

14 clinical trials for this condition and its sub-types, 0 tagged with Dystonia 5 itself.

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↑ GTP cyclohydrolase I deficiency (1) ↑ Autosomal dominant dopa-responsive dystonia (0)

Including sub-types (14) Tagged with Dystonia 5 (0)

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