Tryptasemia.com and Tryptasemia.org were created to help people find information about Hereditary Alpha Tryptasemia Syndrome quickly. Much of what can be found on a quick search includes scientific papers and Facebook groups which are closed.
"Tryptasemia" has been used as a name for the website, because the term "Hereditary Alpha Tryptasemia Syndrome" still seems to be somewhat fluid, as of July 2019. United States researchers tend to refer to it as Hereditary Alpha Tryptasemia Syndrome, while those in other countries are likely to refer to it as Familial Hypertryptasemia. Additionally, insurance companies cannot accurately reflect this condition, until it is added into the ICD-10 code list.
There will be no intent to replicate information stored elsewhere. Wherever possible, there will be links to that information.
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