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Target

1) Patients with coagulated symgenetic hypophosphatemia.


2) Understand the needs and demands of patients, and encourage and promote mutual assistance and self-reliance among patients.

3) Enhance patients' and the general public's correct understanding of X-linked genetic hypophosphatemia and promote communication and exchange between patients and all sectors of society.

4) Strengthen ties with government departments, service providers and professional groups to work together to improve patients’ diagnosis, treatment, rehabilitation and quality of life.

5) Promote and support scientific and medical research on X-linked genetic hypophosphatemia and publish the research results to the public.

6) Establish working relationships with relevant overseas organizations to promote mutual exchange and cooperation.

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Welcome to join us for more information

© 2026 Hong Kong X-linked Hypophosphatemia Association is a validly registered charitable organization exempt from taxation under Section 88 of the Inland Revenue Ordinance. Registration No. 91/20231.

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