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mukopolysacharidózy
Č. záznamu d009083 Dátum 06.06.2025 Typ M Tematický termín mukopolysacharidózy MDT C16.320.565.202.715C16.320.565.595.600C17.300.550.575C18.452.648.202.715C18.452.648.595.600 Poznámka Group 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. predmetové heslo
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