X-linked mental retardation Lesch-Nyhan syndrome MSH2010_2010_02_22:D007926 URI: http://www.ebi.ac.uk/cellline#Lesch-Nyhan_syndrome SNOMEDCT_2010_1_31:190918000 SNOMEDCT_2010_1_31:190921003 UMLS_CUI:C0023374 "Hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder)" EXACT [SNOMEDCT_2005_07_31:267451005] SNOMEDCT_2010_1_31:90924007 SNOMEDCT_2010_1_31:190917005 SNOMEDCT_2010_1_31:267451005 SNOMEDCT_2010_1_31:124275001 OMIM2009_05_01:300322 "Complete hypoxanthine-guanine phosphoribosyltransferase deficiency" EXACT [SNOMEDCT_2005_07_31:190921003] "Lesch-Nyhan syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:10406007] "Hypoxanthine-guanine-phosphoribosyltransferase deficiency (& [Lesch - Nyhan syndrome])" EXACT [SNOMEDCT_2005_07_31:190918000] "hypoxanthine guanine phosphoribosyltransferase deficiency" EXACT [CSP2005:1849-8105] SNOMEDCT_2010_1_31:68655008 "deficiency of IMP pyrophosphorylase" EXACT [SNOMEDCT_2005_07_31:124275001] "X-linked hyperuricemia (disorder) [Ambiguous]" EXACT [SNOMEDCT_2005_07_31:68655008] SNOMEDCT_2010_1_31:10406007 NCI2009_04D:C61255 "Lesch - Nyhan syndrome" EXACT [SNOMEDCT_2005_07_31:190917005] "Hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder) [Ambiguous]" EXACT [SNOMEDCT_2005_07_31:90924007] "HG-PRT deficiency" EXACT [MTHICD9_2006:277.2] hyperuricemia syndrome inborn metabolic brain disease