mucopolysaccharidosis SNOMEDCT_2010_1_31:267452003 URI: http://www.ebi.ac.uk/cellline#mucopolysaccharidosis SNOMEDCT_2010_1_31:11380006 "Mucopolysaccharidosis [Ambiguous]" EXACT [SNOMEDCT_2005_07_31:267452003] SNOMEDCT_2010_1_31:190942001 "Mucopolysaccharidosis" EXACT [ICD9CM_2006:277.5] SNOMEDCT_2010_1_31:190936000 MSH2010_2010_02_22:D009083 "Mucopolysaccharidoses" EXACT [] "mucopolysaccharidosis" EXACT [CSP2005:1849-6106] UMLS_CUI:C0026703 "Mucopolysaccharidosis (disorder)" EXACT [SNOMEDCT_2005_07_31:11380006] "Mucopolysaccharidosis is a lysosomal storage disease described as any of a group of genetically determined disorder (as Hunter's syndrome and Hurler's syndrome) of glycosaminoglycan metabolism that are characterized by the accumulation of glycosaminoglycans in the tissues and their excretion in the urine." [URL:http\://www2.merriam-webster.com/cgi-bin/mwmednlm?book=Medical&va=Mucopolysaccharidosis] ICD9CM_2010:277.5 "Mucopolysaccharidosis" EXACT [SNOMEDCT_2005_07_31:190936000] NCI2009_04D:C61259 "Mucopolysaccharidosis NOS (disorder)" EXACT [SNOMEDCT_2005_07_31:190942001] inborn errors carbohydrate metabolism mucinoses lysosomal storage disease