ONKI3 | Medical Subject Headings

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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 ∟ Cystinuria 1 coordinate concept ∟ Hartnup Disease Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Female Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias ∟ Cystinuria 1 coordinate concept ∟ Hartnup Disease Medical Subject Headings (MeSH) ∟ Male Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias ∟ Cystinuria 1 coordinate concept ∟ Hartnup Disease Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias ∟ Cystinuria 1 coordinate concept ∟ Hartnup Disease 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 ∟ Cystinuria Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Female Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias ∟ Cystinuria Medical Subject Headings (MeSH) ∟ Male Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias ∟ Cystinuria Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Renal Aminoacidurias ∟ Cystinuria 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 Aminoacidurias > Renal Tubular Transport, Inborn Errors > Kidney Diseases > Urologic Diseases > Female Urogenital Diseases > Female Urogenital Diseases and Pregnancy Complications > Medical Subject Headings (MeSH) Renal Aminoacidurias > Renal Tubular Transport, Inborn Errors > Kidney Diseases > Urologic Diseases > Male Urogenital Diseases > Medical Subject Headings (MeSH) Renal Aminoacidurias > Renal Tubular Transport, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) X
Scope note:	An inherited disorder due to defective reabsorption of CYSTINE and other BASIC AMINO ACIDS by the PROXIMAL RENAL TUBULES. This form of aminoaciduria is characterized by the abnormally high urinary levels of cystine; LYSINE; ARGININE; and ORNITHINE. Mutations involve the amino acid transport protein gene SLC3A1. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Hartnup Disease X
URI:	X
Labels and equivalent concepts:	Kystinuria (fi) Kystiinivirtsaisuus (fi, replaced) Cystinuri (sv) Cystinuria (la-FI, replaced) X
Share:	X