In this prospective, observational, long term registry patients of all ages with a diagnosis of hypophosphatasia (HPP) are followed at participating sites in multiple countries.
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Natural History Information
Timeframe: 1 Year
Burden of Disease/Patient-reported Outcomes
Timeframe: 1 year
Characterize the epidemiology of the HPP population.
Timeframe: 1 year
Long-Term Safety and Effectiveness of Asfotase Alfa
Timeframe: 1 year