Striatal degeneration, autosomal dominant 2

MONDO:0014835

Any striatal degeneration, autosomal dominant in which the cause of the disease is a mutation in the PDE10A gene.

Also known as: striatal degeneration, autosomal dominant, ADSD2, PDE10A striatal degeneration, autosomal dominant, striatal Degeneration, autosomal dominant 2, striatal Degeneration, autosomal dominant type 2, striatal degeneration, autosomal dominant 2; ADSD2, striatal degeneration, autosomal dominant caused by mutation in PDE10A

12 clinical trials for this condition and its sub-types, 0 tagged with Striatal degeneration, autosomal dominant 2 itself.

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↑ Striatal degeneration, autosomal dominant (0)

Including sub-types (12) Tagged with Striatal degeneration, autosomal dominant 2 (0)

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