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Illness finder is a diagnostic medicine tool for educational purpose that looks up your patients' health conditions or symptoms and diagnosis and find diseases or illnesses based on chosen gender, age, risk factors, illness, signs, symptoms and prevalence. Illnessfinder is inspired by Evidence based medicine (EMB) and healthcare that aims to apply the best (most reliable) knowledge that is available at decision time. Illnessfinder aims to free up time for the therapeutic dialogue and ensure quality at the evidence based practice, uniting proven medical findings and clinical evidence with systematised data technology.
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| Mucopolysaccharidosis VI | Legal notice |
Other terms
Mucopolysaccharidosis VIs,Polydystrophic Dwarfism,Dwarfism, Polydystrophic,Mucopolysaccharidosis Type 6,6, Mucopolysaccharidosis Type,Mucopolysaccharidosis Type 6s,Type 6, Mucopolysaccharidosis,Type 6s, Mucopolysaccharidosis,Maroteaux-Lamy Syndrome,Maroteaux Lamy Syndrome,Syndrome, Maroteaux-Lamy,Mucopolysaccharidosis 6,Arylsulfatase B Deficiency,Arylsulfatase B Deficiencies,Deficiencies, Arylsulfatase B,Deficiency, Arylsulfatase B,N-Acetylgalactosamine-4-Sulfatase Deficiency,Deficiencies, N-Acetylgalactosamine-4-Sulfatase,Deficiency, N-Acetylgalactosamine-4-Sulfatase,N-Acetylgalactosamine-4-Sulfatase Deficiencies
Description
Mucopolysaccharidosis VI: 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).
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The version of the data is 2010 MeSH. Last reviewed April 26, 2010. No modification has been made in the content of the file.
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