Congenital Disorder

Hypophosphatemia, Familial

AMW:DIS:120150

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.

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Hypophosphatemia, Familial has parent Hypophosphatemia

Familial Hypophosphatemic Rickets has parent Hypophosphatemia, Familial

Hypophosphatemia, Familial has parent Metal Metabolism, Inborn Errors

Hypophosphatemia, Familial has parent Renal Tubular Transport, Inborn Errors

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