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<p>The United Kingdom Haemophilia Centre Doctors’ Organisation is required by the
Department of Health and Social Care to collect data on diagnosis, management and
complications of bleeding disorders including number of bleeds. This information is
kept in the National Haemophilia Database (NHD) and funded by NHS England. The dataset
can be found on the NHD website at the following link:</p><p> </p><p><a href="http://www.ukhcdo.org/wp-content/uploads/2018/12/NHD_HT_DataSet_2018_Final.pdf"
target="_blank">http://www.ukhcdo.org/wp-content/uploads/2018/12/NHD_HT_DataSet_2018_Final.pdf</a></p>
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