Medical Definition of Type VII mucopolysaccharidosis
1.
An autosomal recessive disorder due to a deficiency of a beta-glucuronidase; defective lysosomal degradation of dermatan sulfate, heparan sulfate, and chondroitin sulfate; cellular function disrupted in most tissues.
Synonym: type VII mucopolysaccharidosis, type VIII mucopolysaccharidosis.
(05 Mar 2000)
Lexicographical Neighbors of Type VII Mucopolysaccharidosis
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