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Skin and Connective Tissue Diseases > Connective Tissue Diseases > Mucinoses > Mucopolysaccharidoses > Mucopolysaccharidosis VII
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lysosomal Storage Diseases > Mucopolysaccharidoses > Mucopolysaccharidosis VII
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lysosomal Storage Diseases > Mucopolysaccharidoses > Mucopolysaccharidosis VII
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Mucopolysaccharidoses > Mucopolysaccharidosis VII
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Mucopolysaccharidoses > Mucopolysaccharidosis VII

Preferred term

Mucopolysaccharidosis VII  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • beta-Glucuronidase Deficiencies
  • beta Glucuronidase Deficiency
  • beta-Glucuronidase Deficiency
  • Deficiencies, beta-Glucuronidase
  • Deficiencies, GUSB
  • Deficiency, beta-Glucuronidase
  • Deficiency, GUSB
  • Disease, Sly
  • GUSB Deficiencies
  • GUSB Deficiency
  • Mucopolysaccharidosis 7
  • Mucopolysaccharidosis Type VII
  • Mucopolysaccharidosis Type VIIs
  • Sly Disease
  • Sly Syndrome
  • Syndrome, Sly
  • Type VII, Mucopolysaccharidosis
  • Type VIIs, Mucopolysaccharidosis

Scope note

  • Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase.

History note

  • 92

In other languages

URI

http://www.yso.fi/onto/mesh/D016538

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