Familial Hypophosphatemic Rickets D053098

Related MeSH Hierarchy (12)

Diseases [C] » Musculoskeletal Diseases [C05] » Bone Diseases » Bone Diseases, Metabolic » Rickets » Rickets, Hypophosphatemic » Familial Hypophosphatemic Rickets

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Bone Diseases, Metabolic » Rickets » Rickets, Hypophosphatemic » Familial Hypophosphatemic Rickets

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Calcium Metabolism Disorders » Rickets » Rickets, Hypophosphatemic » Familial Hypophosphatemic Rickets

Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Hypophosphatemia, Familial » Familial Hypophosphatemic Rickets

Description

A hereditary disorder characterized by HYPOPHOSPHATEMIA; RICKETS; OSTEOMALACIA; renal defects in phosphate reabsorption and vitamin D metabolism; and growth retardation. Autosomal and X-linked dominant and recessive variants have been reported.   MeSH

Phase 3 Indicated Drugs (3)

Phase 1 Indicated Drugs (1)

Other Experimental Indicated Drugs (3)


Organization Involved with Phase 2 Indications (1)

Organization Involved with Phase 1 Indications (4)

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UMLS Data


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