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mucopolysaccharidosis (MPS)
Specific
galactosialidosis (Goldberg syndrome)
Hunter syndrome; mucopolysaccharidosis-2; MPS2
Hurler-Scheie syndrome; mucopolysaccharidosis-1 & 5; Pfaundler Hurler syndrome; MPS1; MPS5
Maroteaux-Lamy syndrome; polydystrophic dwarfism; mucopolysaccharidosis-6; MPS6
Morquio disease; mucopolysaccharidosis-4; eccentro-osteochondrodysplasia; MPS4
mucopolysaccharidosis 9 (hyaluronidase deficiency)
mucopolysaccharidosis-7; Sly syndrome; MPS7
Sanfillipo syndrome; mucopolysaccharidosis-3; polydystrophic oligophrenia; MPS3
sialidosis; mucolipidosis 1; lipomucopolysaccharidosis; sialidase deficiency; glycoprotein neuraminidase deficiency; neuraminidase 1 deficiency; cherry red spot-myoclonus syndrome
General
carbohydrate inborn error of metabolism
lysosomal storage disease
References
- National Institute of Neurological Disorders and Stroke (NINDS)
NINDS Mucopolysaccharidoses Information Page
https://www.ninds.nih.gov/Disorders/All-Disorders/Mucopolysaccharidoses-Information-Page