Wilson disease
MONDO:0010200A 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
50 clinical trials for this condition and its sub-types.
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Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn errors of metabolism
(42)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Inborn metal metabolism disorder
(1)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
Disorder of copper metabolism
(0)