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The Thai FH registry is a database where physicians/researchers collected medical information from FH patients, in order to gather more understanding of the disease and to provide the best practice to those living with FH.

Thai FH registry was started in August 2018 after Thailand officially joined the EAS FH Studies Collaboration (FHSC) , which is an international secure warehouse of FH Data, collected and merged from all the countries included in the global network (currently 70 countries). This global registry is the first example of Big Data on FH currently available.

SC-THA-NP-00267 SEP 2023

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