Medical Definition of Type i h/s mucopolysaccharidosis

1. Although clinically distinct diseases, fibroblasts from patients with Hurler syndrome and with Scheie syndrome do not cross complement in culture, suggesting that the enzyme defect is the same. This entry appears with permission from the Dictionary of Cell and Molecular Biology (11 Mar 2008)

Lexicographical Neighbors of Type I H/s Mucopolysaccharidosis

type IV acrocephalosyndactyly
type IV allergic reaction
type IV collagen
type IV familial hyperlipoproteinaemia
type IV prepilin peptidase
type I acrocephalosyndactyly
type I allergic reaction
type I cells
type I collagen
type I diabetes
type I diabetes
type I diabetes mellitus
type I dip
type i error
type I familial hyperlipoproteinaemia
type I H/S mucopolysaccharidosis
type I hyperlipoproteinaemia
type I interferon
type I mortality
type locality
type material
type metal
type O
type of architecture
type series
type species
type species
type specimen
type specimen
type strain

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