disease has basis in dysfunction of ATP7B inborn metal metabolism disorder Wilson disease DOID:893 GARD:0007893 ICD10:E83.0 ICD10:E83.01 MESH:D006527 MONDO:0010200 MedDRA:10019819 NCIT:C84756 OMIM:277900 Orphanet:905 SCTID:88518009 UMLS:C0019202 WD Westphal pseudosclerosis Westphal-Strumpell syndrome Wilson disease Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body. Wilson's disease Wnd cerebral pseudosclerosis hepatolenticular Degeneration hepatolenticular degeneration https://rarediseases.info.nih.gov/diseases/7893/wilson-disease rare hereditary metabolic disease with peripheral neuropathy metal transport or utilization disorder with epilepsy disorder of copper metabolism rare disorder with dystonia and other neurologic or systemic manifestation neurometabolic disease nephropathy secondary to a storage or other metabolic disease rare neurologic disease with psychiatric involvement supranuclear oculomotor palsy metabolic disease with corneal opacity metabolic disease with cataract