Medical Definition of Type I hyperlipoproteinaemia

1. An rare inherited disorder where there is a deficiency of an enzyme (lipoprotein lipase) which breaks down fat molecules, causing the accumulation of fats or lipoproteins in the blood. Symptoms in infancy include abdominal pain (appears as if its colic), failure to thrive and skin lesions (xanthomas). Origin: Gr. Haima = blood (27 Sep 1997)

Lexicographical Neighbors of Type I Hyperlipoproteinaemia

type IV allergic reaction
type IV familial hyperlipoproteinaemia
type IV prepilin peptidase
type I H/S 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 (current term)
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

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