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Acidosis, Renal Tubular
MeSH HeadingAcidosis, Renal Tubular
Tree NumberC12.777.419.815.093
Tree NumberC13.351.968.419.815.093
Tree NumberC16.320.565.861.093
Tree NumberC18.452.076.176.210
Tree NumberC18.452.648.861.093
Scope NoteA 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.
Entry TermAcidosis, Renal Tubular, Type I
Entry TermAcidosis, Renal Tubular, Type II
Entry TermAutosomal Dominant Distal Renal Tubular Acidosis
Entry TermClassic Distal Renal Tubular Acidosis
Entry TermDistal Renal Tubular Acidosis
Entry TermProximal Renal Tubular Acidosis
Entry TermRenal Tubular Acidosis
Entry TermRenal Tubular Acidosis 1
Entry TermRenal Tubular Acidosis I
Entry TermRenal Tubular Acidosis II
Entry TermRenal Tubular Acidosis, Distal, Autosomal Dominant
Entry TermRenal Tubular Acidosis, Proximal
Entry TermRenal Tubular Acidosis, Proximal, with Ocular Abnormalities
Entry TermRenal Tubular Acidosis, Type I
Entry TermRenal Tubular Acidosis, Type II
Entry TermRTA, Classic Type
Entry TermRTA, Distal Type, Autosomal Dominant
Entry TermRTA, Gradient Type
Entry TermRTA, Proximal Type
Entry TermType I Renal Tubular Acidosis
Entry TermType II Renal Tubular Acidosis
Allowable QualifiersBL CF CI CL CN CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
History Note65
Date of Entry19990101
Unique IDD000141


MeSH Tree Structures

 
Male Urogenital Diseases [C12]
   Urologic Diseases [C12.777]
      Kidney Diseases [C12.777.419]
         Renal Tubular Transport, Inborn Errors [C12.777.419.815]
Arrow pointing to current tree nodeAcidosis, Renal Tubular [C12.777.419.815.093]
Bartter Syndrome [C12.777.419.815.279]
Dent Disease [C12.777.419.815.364]
Fanconi Syndrome [C12.777.419.815.450]
Gitelman Syndrome [C12.777.419.815.491]
Glycosuria, Renal [C12.777.419.815.532]
Hypophosphatemia, Familial [C12.777.419.815.647]  +
Liddle Syndrome [C12.777.419.815.683]
Oculocerebrorenal Syndrome [C12.777.419.815.720]
Pseudohypoaldosteronism [C12.777.419.815.770]
Renal Aminoacidurias [C12.777.419.815.885]  +

 
Female Urogenital Diseases and Pregnancy Complications [C13]
   Female Urogenital Diseases [C13.351]
      Urologic Diseases [C13.351.968]
         Kidney Diseases [C13.351.968.419]
            Renal Tubular Transport, Inborn Errors [C13.351.968.419.815]
Arrow pointing to current tree nodeAcidosis, Renal Tubular [C13.351.968.419.815.093]
Bartter Syndrome [C13.351.968.419.815.279]
Dent Disease [C13.351.968.419.815.364]
Fanconi Syndrome [C13.351.968.419.815.450]
Gitelman Syndrome [C13.351.968.419.815.491]
Glycosuria, Renal [C13.351.968.419.815.532]
Hypophosphatemia, Familial [C13.351.968.419.815.647]  +
Liddle Syndrome [C13.351.968.419.815.683]
Oculocerebrorenal Syndrome [C13.351.968.419.815.720]
Pseudohypoaldosteronism [C13.351.968.419.815.770]
Renal Aminoacidurias [C13.351.968.419.815.885]  +

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Metabolism, Inborn Errors [C16.320.565]
         Renal Tubular Transport, Inborn Errors [C16.320.565.861]
Arrow pointing to current tree nodeAcidosis, Renal Tubular [C16.320.565.861.093]
Dent Disease [C16.320.565.861.271]
Fanconi Syndrome [C16.320.565.861.450]
Gitelman Syndrome [C16.320.565.861.491]
Glycosuria, Renal [C16.320.565.861.532]
Hypophosphatemia, Familial [C16.320.565.861.647]  +
Liddle Syndrome [C16.320.565.861.698]
Oculocerebrorenal Syndrome [C16.320.565.861.750]
Pseudohypoaldosteronism [C16.320.565.861.770]
Renal Aminoacidurias [C16.320.565.861.885]  +

 
Nutritional and Metabolic Diseases [C18]
   Metabolic Diseases [C18.452]
      Acid-Base Imbalance [C18.452.076]
         Acidosis [C18.452.076.176]
Acidosis, Lactic [C18.452.076.176.180]
Arrow pointing to current tree nodeAcidosis, Renal Tubular [C18.452.076.176.210]
Acidosis, Respiratory [C18.452.076.176.310]
Ketosis [C18.452.076.176.652]  +

 
Nutritional and Metabolic Diseases [C18]
   Metabolic Diseases [C18.452]
      Metabolism, Inborn Errors [C18.452.648]
         Renal Tubular Transport, Inborn Errors [C18.452.648.861]
Arrow pointing to current tree nodeAcidosis, Renal Tubular [C18.452.648.861.093]
Dent Disease [C18.452.648.861.271]
Fanconi Syndrome [C18.452.648.861.450]
Gitelman Syndrome [C18.452.648.861.491]
Glycosuria, Renal [C18.452.648.861.532]
Hypophosphatemia, Familial [C18.452.648.861.647]  +
Liddle Syndrome [C18.452.648.861.698]
Oculocerebrorenal Syndrome [C18.452.648.861.750]
Pseudohypoaldosteronism [C18.452.648.861.770]
Renal Aminoacidurias [C18.452.648.861.885]  +

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