Related MeSH Hierarchy (7)
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Hypophosphatemia, Familial
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Hypophosphatemia, Familial
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Hypophosphatemia, Familial
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Hypophosphatemia, Familial
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Renal Tubular Transport, Inborn Errors » Hypophosphatemia, Familial
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Hypophosphatemia, Familial
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Phosphorus Metabolism Disorders » Hypophosphatemia » Hypophosphatemia, Familial
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. MeSH
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Subtype Terms (1)
Familial Hypophosphatemic Rickets
13 drugs (9 approved, 4 experimental)
Approved Indicated Drugs (2)
Phase 3 Indicated Drugs (1)
Other Experimental Indicated Drugs (2)
Organization Involved with Phase 3 Indications (2)
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UMLS Data
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