ONKI3 | Medical Subject Headings

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Bartter Syndrome

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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 ∟ Bartter Syndrome 8 coordinate concepts ∟ Acidosis, Renal Tubular \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias Medical Subject Headings (MeSH) ∟ Endocrine System Diseases ∟ Adrenal Gland Diseases ∟ Adrenocortical Hyperfunction ∟ Hyperaldosteronism ∟ Bartter Syndrome 8 coordinate concepts ∟ Acidosis, Renal Tubular \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Female Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Bartter Syndrome 8 coordinate concepts ∟ Acidosis, Renal Tubular \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias Medical Subject Headings (MeSH) ∟ Male Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Bartter Syndrome 8 coordinate concepts ∟ Acidosis, Renal Tubular \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Bartter Syndrome 8 coordinate concepts ∟ Acidosis, Renal Tubular \| ∟ Fanconi Syndrome \| ∟ Gitelman Syndrome \| ∟ Glycosuria, Renal \| ∟ Hypophosphatemia, Familial \| ∟ Oculocerebrorenal Syndrome \| ∟ Pseudohypoaldosteronism \| ∟ Renal Aminoacidurias 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 ∟ Bartter Syndrome Medical Subject Headings (MeSH) ∟ Endocrine System Diseases ∟ Adrenal Gland Diseases ∟ Adrenocortical Hyperfunction ∟ Hyperaldosteronism ∟ Bartter Syndrome Medical Subject Headings (MeSH) ∟ Female Urogenital Diseases and Pregnancy Complications ∟ Female Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Bartter Syndrome Medical Subject Headings (MeSH) ∟ Male Urogenital Diseases ∟ Urologic Diseases ∟ Kidney Diseases ∟ Renal Tubular Transport, Inborn Errors ∟ Bartter Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Renal Tubular Transport, Inborn Errors ∟ Bartter Syndrome Renal Tubular Transport, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Hyperaldosteronism > Adrenocortical Hyperfunction > Adrenal Gland Diseases > Endocrine System Diseases > 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
historyNote*:	2005 (1975) X
publicMeSHNote*:	2005; see BARTTER'S DISEASE 1991-2004, see HYPERALDOSTERONISM 1975-1990 X
Scope note:	A group of disorders caused by the defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA, hypercalciuria, metabolic ALKALOSIS, and hyper-reninemic HYPERALDOSTERONISM without HYPERTENSION. There are several subtypes resulting from mutations of autosomal recessive genes for SODIUM-POTASSIUM-CHLORIDE COTRANSPORTERS. X
activeMeSHYear*:	2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Acidosis, Renal Tubular \| Fanconi Syndrome \| Gitelman Syndrome \| Glycosuria, Renal \| Hypophosphatemia, Familial \| Oculocerebrorenal Syndrome \| Pseudohypoaldosteronism \| Renal Aminoacidurias X
URI:	X
Labels and equivalent concepts:	Bartterin oireyhtymä (fi) Bartterin tauti (fi, replaced) Bartterin syndrooma (fi, replaced) Bartters sjukdom (sv) Bartters syndrom (sv, replaced) Barter's Disease (en, replaced) Bartter Disease (en, replaced) Bartter's Disease (en, replaced) Barter Disease (en, replaced) Morbus Bartter (la-FI, replaced) Syndroma Bartter (la-FI, replaced) X
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