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bn:01273849n
Noun Concept
Categories: Syndromes affecting the kidneys, Autosomal recessive disorders, Rare syndromes, Membrane transport protein disorders, Kidney diseases
EN
Gitelman syndrome  Familial hypokalemia-hypomagnesemia  Gitelman's syndrome  Gittings syndrome  Hillel Gitelman
EN
Gitelman syndrome is an autosomal recessive kidney tubule disorder characterized by low blood levels of potassium and magnesium, decreased excretion of calcium in the urine, and elevated blood pH. It is the most frequent hereditary salt-losing tubulopathy. Wikipedia
Definitions
Relations
Sources
EN
Gitelman syndrome is an autosomal recessive kidney tubule disorder characterized by low blood levels of potassium and magnesium, decreased excretion of calcium in the urine, and elevated blood pH. It is the most frequent hereditary salt-losing tubulopathy. Wikipedia
An autosomal recessive kidney tubule disorder Wikipedia Disambiguation
Human disease Wikidata
IS A
rare disease
genetic disease
Inborn errors of renal tubular transport
autosomal recessive disease
GENETIC ASSOCIATION
sodium-chloride symporter
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
Gitelman syndrome
Wikidata
EN
Gitelman syndrome
Wikipedia Redirections
EN
Familial hypokalemia-hypomagnesemia, Gittings syndrome, Hillel Gitelman, Hillel J. Gitelman, Hillel Jonathan Gitelman
Wikidata Alias
EN
Familial hypokalemia-hypomagnesemia, Gitelman's syndrome, GITELMAN SYNDROME, HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA, Potassium and Magnesium Depletion, Primary renal tubular hypokalemic hypomagnesemia with hypocalciuria

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