Searchable abstracts of presentations at key conferences in endocrinology

ea0095p55 | Miscellaneous/other 1 | BSPED2023

Phenotyping hypophosphatasia using UK primary care electronic health records

Buendia Orlando , Mahon Hadley , Khan Ghazanfar

Objectives: Hypophosphatasia (HPP) is a rare genetic disorder. Early diagnosis is challenging due to the disease’s complexity and low physician awareness.1 This study aimed to demonstrate how a digital health approach that scans electronic health records (EHR) may lead to earlier diagnosis of HPP.Methods: Patients with HPP were identified in the Optimum Patient Care Research Database (OPCRD), a UK database of 13.7 m...