ONKI3 | Medical Subject Headings

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Acidosis, Renal Tubular

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Acidosis, Renal Tubular 12 coordinate concepts ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias \| ∟ Acidosis, Lactic \| ∟ Acidosis, Respiratory \| ∟ Diabetic Ketoacidosis \| ∟ Ketosis Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Female Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Acidosis, Renal Tubular 12 coordinate concepts ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias \| ∟ Acidosis, Lactic \| ∟ Acidosis, Respiratory \| ∟ Diabetic Ketoacidosis \| ∟ Ketosis Medical Subject Headings (MeSH) ∟ Male Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Acidosis, Renal Tubular 12 coordinate concepts ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias \| ∟ Acidosis, Lactic \| ∟ Acidosis, Respiratory \| ∟ Diabetic Ketoacidosis \| ∟ Ketosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Acid-Base Imbalance ∟ Acidosis ∟ Acidosis, Renal Tubular 12 coordinate concepts ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias \| ∟ Acidosis, Lactic \| ∟ Acidosis, Respiratory \| ∟ Diabetic Ketoacidosis \| ∟ Ketosis Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Acidosis, Renal Tubular 12 coordinate concepts ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias \| ∟ Acidosis, Lactic \| ∟ Acidosis, Respiratory \| ∟ Diabetic Ketoacidosis \| ∟ Ketosis X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Acidosis, Renal Tubular Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Female Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Acidosis, Renal Tubular Medical Subject Headings (MeSH) ∟ Male Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Acidosis, Renal Tubular Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Acid-Base Imbalance ∟ Acidosis ∟ Acidosis, Renal Tubular Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Acidosis, Renal Tubular Renal Tubular Transport, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Renal Tubular Transport, Inborn Errors > Kidney Diseases > Urologic Diseases > Female Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Medical Subject Headings (MeSH) Renal Tubular Transport, Inborn Errors > Kidney Diseases > Urologic Diseases > Male Urogenital Diseases > Medical Subject Headings (MeSH) Acidosis > Acid-Base Imbalance > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Renal Tubular Transport, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
historyNote*:	65 X
publicMeSHNote*:	65 X
Scope note:	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. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1965-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Bartter Syndrome \| Fanconi Syndrome \| Gitelman Syndrome \| Glycosuria, Renal \| Hypophosphatemia, Familial \| Oculocerebrorenal Syndrome \| Pseudohypoaldosteronism \| Renal Aminoacidurias \| Acidosis, Lactic \| Acidosis, Respiratory \| Diabetic Ketoacidosis \| Ketosis X
URI:	X
Labels and equivalent concepts:	Renaalinen tubulaarinen asidoosi (fi) Asidoosi, renaalinen tubulaarinen (fi, replaced) Munuaisperäinen asidoosi (fi, replaced) Acidos, renal tubulär (sv) Renal tubulär acidos (sv, replaced) Type II Renal Tubular Acidosis (en, replaced) Type I Renal Tubular Acidosis (en, replaced) Renal Tubular Acidosis, Proximal, with Ocular Abnormalities (en, replaced) Acidosis, Renal Tubular, Type II (en, replaced) Classic Distal Renal Tubular Acidosis (en, replaced) Renal Tubular Acidosis (en, replaced) Renal Tubular Acidosis, Distal, Autosomal Dominant (en, replaced) Acidosis, Renal Tubular, Type I (en, replaced) X
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