Related MeSH Hierarchy (6)
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Renal Tubular Transport, Inborn Errors
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Renal Tubular Transport, Inborn Errors
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Renal Tubular Transport, Inborn Errors
Description
Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES. MeSH
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Subtype Terms (11)
Acidosis, Renal Tubular
6 drugs (5 approved, 1 experimental)
Dent Disease
2 approved drugs
Fanconi Syndrome
1 approved drug
Gitelman Syndrome
2 drugs (1 approved, 1 experimental)
Hypophosphatemia, Familial
5 drugs (4 approved, 1 experimental)
Pseudohypoaldosteronism
4 drugs (3 approved, 1 experimental)
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UMLS Data
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