Hypophosphatasia (HPP) is a rare inherited metabolic disease characterized by alkaline phosphatase (ALP) enzyme deficiency caused by loss-of-function mutations in the gene (1p36.1-34) encoding tissue non-specific alkaline phosphatase (TNSALP) enzyme.
Would you like to bring hope to hypophosphatasia patients?
HIFO-DER was founded in December 2019 with the mission of raising awareness of hypophosphatasia, a rare disease worldwide.
By becoming a member of our association, you can support the fight against hypophosphatasia. Our members can participate in association activities and have a say in important decisions.
You can support our activities by donating your time and talent. Our volunteers are bringing hope and making a difference to hypophosphatasia patients and their families.
You can contribute to the treatment of patients diagnosed with hypophosphatasia with your financial donation. Every donation is an important step toward changing a life.
