Paroxysmal nonkinesigenic dyskinesia 1

MONDO:0700089

Paroxysmal nonkinesigenic dyskinesia in which the cause of the disease is a mutation in the PNKD gene.

Also known as: PNKD paroxysmal dyskinesia, PxMD-PNKD, paroxysmal dyskinesia caused by mutation in PNKD, paroxysmal nonkinesigenic dyskinesia 1, paroxysmal nonkinesigenic dyskinesia type 1, PNKD1, choreoathetosis, familial paroxysmal, choreoathetosis, nonkinesigenic

15 clinical trials for this condition and its sub-types, 1 tagged with Paroxysmal nonkinesigenic dyskinesia 1 itself.

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Where it sits in the disease tree

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↑ Paroxysmal nonkinesigenic dyskinesia (1)

Including sub-types (15) Tagged with Paroxysmal nonkinesigenic dyskinesia 1 (1)

Completed 1

Could a common mineral ease rare genetic disorder? zinc trial shows promise

Disease control Completed

This pilot trial tested whether taking oral zinc every day for 6 months is safe and doable for people with GNAO1 disorders, a rare genetic condition that causes movement problems, seizures, and developmental delays. 13 participants aged 6 months to 30 years took zinc acetate. The…

Phase 2 • Sponsor: Children's University Hospital Cologne, Germany • Aim: Disease control

Last updated Jun 27, 2026 09:01 UTC

Paroxysmal nonkinesigenic dyskinesia 1

Where it sits in the disease tree

Could a common mineral ease rare genetic disorder? zinc trial shows promise