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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 II | Legal notice |
Other terms
IIs, Mucopolysaccharidosis,Mucopolysaccharidosis IIs,Mucopolysaccharidosis Type 2,2, Mucopolysaccharidosis Type,2s, Mucopolysaccharidosis Type,Mucopolysaccharidosis Type 2s,Type 2, Mucopolysaccharidosis,Type 2s, Mucopolysaccharidosis,Hunter's Syndrome,Hunter Syndrome,Hunters Syndrome,Syndrome, Hunter's,Mucopolysaccharidosis 2,Gargoylism, Hunter Syndrome,Hunter Syndrome Gargoylism,Sulfoiduronate Sulfatase Deficiency,Deficiencies, Sulfoiduronate Sulfatase,Deficiency, Sulfoiduronate Sulfatase,Sulfatase Deficiencies, Sulfoiduronate,Sulfatase Deficiency, Sulfoiduronate,Sulfoiduronate Sulfatase Deficiencies,Iduronate Sulfatase Deficiency,Deficiencies, Iduronate Sulfatase,Deficiency, Iduronate Sulfatase,Iduronate Sulfatase Deficiencies,Sulfatase Deficiencies, Iduronate,Sulfatase Deficiency, Iduronate,Iduronate 2-Sulfatase Deficiency,Deficiencies, Iduronate 2-Sulfatase,Deficiency, Iduronate 2-Sulfatase,Iduronate 2 Sulfatase Deficiency,Iduronate 2-Sulfatase Deficiencies
Description
Mucopolysaccharidosis II: Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.
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- Mental Retardation, X-Linked
- Mental Retardation, X-Linked
- Mental Retardation, X-Linked
- Mucopolysaccharidoses
- Mucopolysaccharidoses
- Mucopolysaccharidoses
- Mucopolysaccharidoses
Legal notice
The U.S. National Library of Medicine is the creator, maintainer, and provider of the data above.
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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