Related MeSH Hierarchy (5)
Diseases [C] » Urogenital Diseases [C12] » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Acidosis, Renal Tubular
Diseases [C] » Urogenital Diseases [C12] » Female Urogenital Diseases and Pregnancy Complications » Female Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Acidosis, Renal Tubular
Diseases [C] » Urogenital Diseases [C12] » Male Urogenital Diseases » Urologic Diseases » Kidney Diseases » Renal Tubular Transport, Inborn Errors » Acidosis, Renal Tubular
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Acid-Base Imbalance » Acidosis » Acidosis, Renal Tubular
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Renal Tubular Transport, Inborn Errors » Acidosis, Renal Tubular
Description
A group of genetic disorders of the KIDNEY TUBULES characterized by the accumulation of metabolically produced acids with elevated plasma chloride, hyperchloremic metabolic ACIDOSIS. Defective renal acidification of URINE (proximal tubules) or low renal acid excretion (distal tubules) can lead to complications such as HYPOKALEMIA, hypercalcinuria with NEPHROLITHIASIS and NEPHROCALCINOSIS, and RICKETS. MeSH
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Approved Indicated Drugs (2)
Phase 3 Indicated Drugs (1)
Other Experimental Indicated Drugs (3)
Organization Involved with Phase 3 Indications (3)
Organization Involved with Other Experimental Indications (1)
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UMLS Data
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