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 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 (current term)
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
type VIII mucopolysaccharidosis

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