Disorder of copper metabolism
MONDO:0017762An 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
54 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn errors of metabolism
(42)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
Disorder of metabolite absorption and transport
(0)
Disorder of mineral absorption and transport
(0)