ONKI3 | Medical Subject Headings

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Renal Aminoacidurias

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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 ∟ Renal Aminoacidurias 8 coordinate concepts 2 subordinate concepts ∟ Cystinuria \| ∟ Hartnup Disease ∟ Acidosis, Renal Tubular \| ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Female Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias 8 coordinate concepts 2 subordinate concepts ∟ Cystinuria \| ∟ Hartnup Disease ∟ Acidosis, Renal Tubular \| ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism Medical Subject Headings (MeSH) ∟ Male Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias 8 coordinate concepts 2 subordinate concepts ∟ Cystinuria \| ∟ Hartnup Disease ∟ Acidosis, Renal Tubular \| ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias 8 coordinate concepts 2 subordinate concepts ∟ Cystinuria \| ∟ Hartnup Disease ∟ Acidosis, Renal Tubular \| ∟ Bartter Syndrome \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism 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 ∟ Renal Aminoacidurias Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Female Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias Medical Subject Headings (MeSH) ∟ Male Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias 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) Renal Tubular Transport, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Cystinuria \| Hartnup Disease X
Annotation:	coordinate IM with specific amino acid /urine (IM) X
historyNote*:	2007 (1963) X
publicMeSHNote*:	2007; see AMINOACIDURIA, RENAL 1965-2006, see AMINOACIDURIA 1963-1964 X
Scope note:	A group of inherited kidney disorders characterized by the abnormally elevated levels of AMINO ACIDS in URINE. Genetic mutations of transport proteins result in the defective reabsorption of free amino acids at the PROXIMAL RENAL TUBULES. Renal aminoaciduria are classified by the specific amino acid or acids involved. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1965-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Related term:	Urine X
Type:	Concept X
Coordinate terms:	Acidosis, Renal Tubular \| Bartter Syndrome \| Fanconi Syndrome \| Gitelman Syndrome \| Glycosuria, Renal \| Hypophosphatemia, Familial \| Oculocerebrorenal Syndrome \| Pseudohypoaldosteronism X
URI:	X
Labels and equivalent concepts:	Renaaliset aminoasiduriat (fi) Renaalinen aminoasiduria (fi, replaced) Munuaisperäinen aminohappovirtsaisuus (fi, replaced) Munuaisperäinen aminoasiduria (fi, replaced) Aminoaciduria, Renal (en, replaced) X
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