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Entry Name Description Category Pathway Gene
H00132 Mucopolysaccharidosis type VII
Sly syndrome 		Mucopolysaccharidosis type VII (MPS7) is an autosomal recessive lysosomal storage disorder caused by deficient activity of beta-glucuronidase in glycosaminoglycan degradation. The enzyme defect results ... Inherited metabolic disorder, Lysosomal disease (MPS7) GUSB [HSA:2990] [KO:K01195]
H00421 Mucopolysaccharidosis Mucopolysaccharidosis (MPS) is a group of lysosomal storage diseases caused by deficient activity of enzymes that play important roles in the degradation of glycosaminoglycans. MPS2/ Hunter syndrome is ... Inherited metabolic disorder, Lysosomal disease (MPS1) IDUA [HSA:3425] [KO:K01217]
(MPS2) IDS [HSA:3423] [KO:K01136]
(MPS3A) SGSH [HSA:6448] [KO:K01565]
(MPS3B) NAGLU [HSA:4669] [KO:K01205]
(MPS3C) HGSNAT [HSA:138050] [KO:K10532]
(MPS3D) GNS [HSA:2799] [KO:K01137]
(MPS4A) GALNS [HSA:2588] [KO:K01132]
(MPS4B) GLB1 [HSA:2720] [KO:K12309]
(MPS6) ARSB [HSA:411] [KO:K01135]
(MPS7) GUSB [HSA:2990] [KO:K01195]
(MPS9) HYAL1 [HSA:3373] [KO:K01197]
(MPS10) ARSK [HSA:153642] [KO:K12376]
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