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Mucopolysaccharidoses

Categorical breakdown of terms falling inder the category of Mucopolysaccharidoses. Sub categories will become more specific in nature to the terms listed for Mucopolysaccharidoses.

Sub-Categories

Terms

Mucopolysaccharidoses - Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in ...

Mucopolysaccharidosis I - Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and c...

Mucopolysaccharidosis II - Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a defi...

Mucopolysaccharidosis III - Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardatio...

Mucopolysaccharidosis IV - Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint ins...

Mucopolysaccharidosis VI - Mucopolysaccharidosis with excessive chondroitin sulfate B in urine, characterized by dwarfism and d...

Mucopolysaccharidosis VII - Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurl...