Multiple Sulfatase Deficiency Disease

MeSH code information
  • Name
  • Concept
    Scope note:An inherited metabolic disorder characterized by the intralysosomal accumulation of sulfur-containing lipids (sulfatides) and MUCOPOLYSACCHARIDES. Excess levels of both substrates are present in urine. This is a disorder of multiple sulfatase (arylsulfatases A, B, and C) deficiency which is caused by the mutation of sulfatase-modifying factor-1. Neurological deterioration is rapid.
  • Tree numbers
    • C10.
    • C16.320.565.189.435.825.850.750
    • C16.320.565.398.641.803.925.750
    • C16.320.565.595.554.825.850.750
    • C18.452.132.100.435.825.850.750
    • C18.452.584.687.803.925.750
    • C18.452.648.189.435.825.850.750
    • C18.452.648.398.641.803.925.750
    • C18.452.648.595.554.825.850.750
Multiple Sulfatase Deficiency Disease - MeSH Info at Gentaur
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