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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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)

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