movement disorder basal ganglia disease inborn metabolic brain disease hepatolenticular degeneration "Wilson's disease" EXACT [SNOMEDCT_2005_07_31:267504005] "Westphal-Strumpell syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:190823004] SNOMEDCT_2010_1_31:192640001 SNOMEDCT_2010_1_31:267504005 SNOMEDCT_2010_1_31:191710006 "Westphal pseudosclerosis" EXACT [CSP2005:1849-4349] "Wilson's disease" EXACT [MTHICD9_2006:275.1] "Cerebral pseudosclerosis (disorder)" EXACT [SNOMEDCT_2005_07_31:192640001] MSH2010_2010_02_22:D006527 SNOMEDCT_2010_1_31:154751003 "Wilson's disease (disorder)" EXACT [SNOMEDCT_2005_07_31:88518009] OMIM2009_05_01:277900 SNOMEDCT_2010_1_31:190823004 SNOMEDCT_2010_1_31:88518009 URI: http://www.ebi.ac.uk/cellline#hepatolenticular_degeneration UMLS_CUI:C0019202 "Wilson's disease * (disorder)" EXACT [SNOMEDCT_2005_07_31:191710006] "Wilson's disease" EXACT [SNOMEDCT_2005_07_31:154751003] nervous system heredodegenerative disease disorder of copper metabolism inborn errors metal metabolism liver disease