Wilson disease

MONDO:0010200

A very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

Also known as: Westphal-Strumpell syndrome, Wilson disease, Wilson's disease, hepatolenticular degeneration, WD, Wnd, hepatolenticular Degeneration

31 clinical trials for this condition and its sub-types, 31 tagged with Wilson disease itself.

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Where it sits in the disease tree

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Part of

↑ Inborn metal metabolism disorder (60) ↑ Disorder of copper metabolism (35)

Including sub-types (31) Tagged with Wilson disease (31)

Trials to join now! 12 Not yet recruiting 6 Not yet finished but already full! 7 Completed 5 Terminated 1

New dialysis device for Wilson's disease tested but trial stopped early

Disease control Stopped early

This trial tested a special dialysis device (MEX-CD1) designed to remove extra copper from the blood of people with Wilson's disease, a genetic condition that causes copper buildup. The study planned to give 5 to 10 treatments over consecutive days and check if the device worked …

Sponsor: Mexbrain • Aim: Disease control

Last updated Jun 27, 2026 08:02 UTC

Wilson disease

Where it sits in the disease tree

New dialysis device for Wilson's disease tested but trial stopped early