Related MeSH Hierarchy (12)
Diseases [C] » Musculoskeletal Diseases [C05] » Bone Diseases » Bone Diseases, Metabolic » Rickets » Rickets, Hypophosphatemic » Familial Hypophosphatemic Rickets
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Renal Tubular Transport, Inborn Errors » Hypophosphatemia, Familial » 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] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Hypophosphatemia, Familial » Familial Hypophosphatemic Rickets
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Phosphorus Metabolism Disorders » Hypophosphatemia » Hypophosphatemia, Familial » Familial Hypophosphatemic Rickets
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Phosphorus Metabolism Disorders » Hypophosphatemia » Rickets, Hypophosphatemic » Familial Hypophosphatemic Rickets
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Nutrition Disorders » Malnutrition » Deficiency Diseases » Avitaminosis » Vitamin D Deficiency » Rickets » Rickets, Hypophosphatemic » Familial Hypophosphatemic Rickets
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 » Familial Hypophosphatemic Rickets
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Hypophosphatemia, Familial » Familial Hypophosphatemic Rickets
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Hypophosphatemia, Familial » Familial Hypophosphatemic Rickets
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Metal Metabolism, 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
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Approved Indicated Drugs (1)
Phase 4 Indicated Drugs (1)
Phase 3 Indicated Drugs (4)
Phase 2 Indicated Drugs (2)
Phase 1 Indicated Drugs (1)
Other Experimental Indicated Drugs (3)
Organization Involved with Phase 4 Indications (3)
Organization Involved with Phase 3 Indications (8)
Organization Involved with Phase 2 Indications (1)
Organization Involved with Phase 1 Indications (4)
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UMLS Data
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