Familial Hypophosphatemia (Phosphate Diabetes)
393
relevant articles (5 outcomes,
23 trials/studies)
found for this Disease
Description:
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.
Also Known As:
Phosphate Diabetes; Phosphaturia; Hypophosphatemia, Familial; Diabetes, Phosphate; Hyperphosphaturia; Familial Hypophosphatemias; Hypophosphatemias, Familial
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Disease Context: Research Results