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)



Type Vii Mucopolysaccharidosis Pictures

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Lexicographical Neighbors of Type Vii Mucopolysaccharidosis

type I acrocephalosyndactyly
type I allergic reaction
type I cells
type I collagen
type I diabetes
type I diabetes mellitus
type I dip
type I error
type I errors
type I familial hyperlipoproteinaemia
type I hyperlipoproteinaemia
type I interferon
type I mortality
type O
type VIII mucopolysaccharidosis
type VII mucopolysaccharidosis
type VI mucopolysaccharidosis
type V acrocephalosyndactyly
type V familial hyperlipoproteinaemia
type V mucopolysaccharidosis
type a personality
type collection
type collections
type culture
type design
type family
type foundry
type genus
type horizon
type host

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