Disorder of copper metabolism

MONDO:0017762

An inherited metabolic disease that is has its basis in the disruption of cellular copper ion homeostasis.

Also known as: inborn cellular copper ion homeostasis disorder, inborn error of cellular copper ion homeostasis, rare inborn error of cellular copper ion homeostasis, copper Transport disorders

35 clinical trials for this condition and its sub-types, 0 tagged with Disorder of copper metabolism itself.

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Where it sits in the disease tree

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Part of

↑ Disorder of mineral absorption and transport (50)

Sub-types of Disorder of copper metabolism

Wilson disease 31 trials
Menkes disease 5 trials
Occipital horn syndrome 1 trial
MEDNIK syndrome 0 trials
Autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect 0 trials
Familial benign copper deficiency 0 trials

Including sub-types (35) Tagged with Disorder of copper metabolism (0)

Trials to join now! 13 Not yet recruiting 6 Not yet finished but already full! 9 Completed 6 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

Disorder of copper metabolism

Where it sits in the disease tree

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