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Mucopolysaccharidosis VI
Definition: Mucopolysaccharidosis with excessive chondroitin sulfate B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-acetylgalactosamine-4-sulfatase (arylsulfatase B).

Synonym(s): Maroteaux-Lamy Syndrome / Polydystrophic Dwarfism / Mucopolysaccharidosis 6 / Dwarfism, Polydystrophic / Maroteaux Lamy Syndrome / Mucopolysaccharidosis VIs / Syndrome, Maroteaux-Lamy / VIs, Mucopolysaccharidosis
MeSH 2010 © U.S. National Library of Medicine®.
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  Web resources for "Mucopolysaccharidosis VI"
             

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view the robot description of the site Mucopolysaccharidosis VI Symptoms, Diagnosis, Treatments and Causes - RightDiagnosis.comwww.wrongdiagnosis.com  
view the robot description of the site Whonamedit - Maroteaux-Lamy syndrome IIwww.whonamedit.com 3
view the robot description of the site Abstract | Mucopolysaccharidosis VIwww.ojrd.com  
view the robot description of the site rare-diseases — National Organization for Rare Disorderswww.rarediseases.org  
 
 

Broader term(s): - Mucopolysaccharidoses - Metabolism, Inborn Errors - Genetic Diseases, Inborn - Congenital, Hereditary, and Neonatal Diseases and Abnormalities

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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy

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  Clinical Trials for "Mucopolysaccharidosis VI"
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Broader term(s): - Mucopolysaccharidoses - Metabolism, Inborn Errors - Congenital, Hereditary, and Neonatal Diseases and Abnormalities

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Subheadings: complications / diagnosis / embryology / epidemiology / etiology / metabolism / microbiology / surgery / therapy


  Broader term(s):
      Diseases
          Nutritional and Metabolic Diseases
              Metabolic Diseases
                  Metabolism, Inborn Errors
                      Lysosomal Storage Diseases
                          Mucopolysaccharidoses 
                      Carbohydrate Metabolism, Inborn Errors
                          Mucopolysaccharidoses 
      Diseases
          Skin and Connective Tissue Diseases
              Connective Tissue Diseases
                  Mucinoses
                      Mucopolysaccharidoses 
      Diseases
          Congenital, Hereditary, and Neonatal Diseases and Abnormalities
              Genetic Diseases, Inborn
                  Metabolism, Inborn Errors
                      Lysosomal Storage Diseases
                          Mucopolysaccharidoses 
                      Carbohydrate Metabolism, Inborn Errors
                          Mucopolysaccharidoses 

MeSH 2010 © U.S. National Library of Medicine®.

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