Number of the records: 1  

mukopolysacharidózy

  1. Record numberd009083
    Date06.06.2025
    TypeM
    Topical termmukopolysacharidózy
    UDCC16.320.565.202.715C16.320.565.595.600C17.300.550.575C18.452.648.202.715C18.452.648.595.600
    NoteGroup of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
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Number of the records: 1  

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