mucopolysaccharidosis (MPS)
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More general terms
More specific terms
- 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
References
- ↑ National Institute of Neurological Disorders and Stroke (NINDS) NINDS Mucopolysaccharidoses Information Page https://www.ninds.nih.gov/Disorders/All-Disorders/Mucopolysaccharidoses-Information-Page