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Hypophosphatemia, Familial
An inherited condition of abnormally low serum levels of PHOSPHATES (below 1 mg/liter) which can occur in a number of genetic diseases with defective reabsorption of inorganic phosphorus by the PROXIMAL RENAL TUBULES. This leads to phosphaturia, HYPOPHOSPHATEMIA, and disturbances of cellular and organ functions such as those in X-LINKED HYPOPHOSPHATEMIC RICKETS; OSTEOMALACIA; and FANCONI SYNDROME.
Subtype terms (1)
More specific conditions that are subtypes of Hypophosphatemia, Familial in the MeSH hierarchy.
- Familial Hypophosphatemic Rickets
15 drugs (10 approved, 5 experimental)
Drugs by status
Approved for this indication (2)
Phase 3 trials (1)
Other trials (2)
Organizations
Organization Involved with Phase 3 Indications (2)