Medical Definition of Type III mucopolysaccharidosis

1. An error of the mucopolysaccharide metabolism, with excretion of large amounts of heparan sulfate in the urine and severe mental retardation with hepatomegaly; skeleton may be normal or may present mild changes similar to those in Hurler's syndrome; several different types (A, B, C, and D) have been identified according to the enzyme deficiency; autosomal recessive inheritance. Synonym: type III mucopolysaccharidosis. (05 Mar 2000)

Lexicographical Neighbors of Type III Mucopolysaccharidosis

type 4 glycogenosis
type 5 glycogenosis
type 6 glycogenosis
type 7 glycogenosis
type A
type AB
type A behaviour
type B
type B behaviour
type IH mucopolysaccharidosis
type III acrocephalosyndactyly
type III collagen
type III familial hyperlipoproteinaemia
type III hyperlipoproteinaemia
type III hypersensitivity reaction
type III mucopolysaccharidosis (current term)
type II acrocephalosyndactyly
type II cells
type II collagen
type II diabetes
type II dip
type II error
type II errors
type II familial hyperlipoproteinaemia
type II hyperlipoproteinaemia
type II interferon
type II mortality
type II mucopolysaccharidosis
type IS mucopolysaccharidosis

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