X-linked Hypophosphatemia (XLH)

Sponsored diagnostic testing programs for X-linked Hypophosphatemia (XLH)

X-linked hypophosphatemia (XLH) is a hereditary disorder of phosphate wasting caused by pathogenic variants in PHEX. It leads to chronically low phosphate levels, resulting in rickets, bone pain, short stature, impaired mobility, and dental abnormalities. Symptoms often begin in childhood, and early diagnosis can improve management and long-term outcomes.

1 program found for X-linked Hypophosphatemia (XLH)

Programs

1 program
X-linked Hypophosphatemia (XLH)Tumor-Induced Osteomalacia (TIO)

Hypophosphatemia

Sponsored by
Kyowa Kirin Inc.

Kyowa Kirin Sponsored Hypophosphatemia 13 Gene Panel

This program offers no-charge genetic testing and counseling for patients in the US and Canada who may have XLH or TIO and meet age and eligibility criteria. It aims to improve diagnostic accuracy, reduce time to confirmation, and support payer coverage needs. No patients, providers, or payers are billed, and program use does not require recommending or prescribing any Kyowa Kirin therapy.

Endocrinology
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Performing labInvitae | Labcorp