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Hereditary alpha tryptasemia syndrome
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==Hereditary alpha tryptasemia/familial hypertryptasemia== '''Hereditary alpha tryptasemia''' (HβΊT or HAT), alternatively known as '''familial hypertryptasemia''' (FHT), is common in the general population, affecting around 1 in 20 people, and is often asymptomatic.<ref name="Lyons2016" /><ref name="niaid-FAQ" /><ref name="Luskin2021" /> Hereditary alpha tryptasemia syndrome (HATS) is only diagnosed when a cluster of associated symptoms are also present.<ref name="niaid-FAQ" />
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