Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Gitelman_syndrome> ?p ?o. }
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- Gitelman_syndrome abstract "Gitelman syndrome is an autosomal recessive kidney disorder characterized by hypokalemic metabolic alkalosis with hypocalciuria, and hypomagnesemia. It is caused by loss of function mutations of the thiazide sensitive sodium-chloride symporter (also known as NCC, NCCT, or TSC) located in the distal convoluted tubule.Gitelman syndrome was formerly considered a subset of Bartter syndrome until the distinct genetic and molecular bases of these disorders were identified. Bartter syndrome is also an autosomal recessive hypokalemic metabolic alkalosis, but it derives from a mutation to the NKCC2 found in the thick ascending limb of the loop of Henle.".
- Gitelman_syndrome diseasesdb "31860".
- Gitelman_syndrome emedicineSubject "article".
- Gitelman_syndrome emedicineTopic "238670".
- Gitelman_syndrome icd10 "N25.8 + E87.6 + E83.4".
- Gitelman_syndrome meshId "D053579".
- Gitelman_syndrome omim "263800".
- Gitelman_syndrome thumbnail Gitelman_syndrome.jpg?width=300.
- Gitelman_syndrome wikiPageExternalLink www.barttersite.org.
- Gitelman_syndrome wikiPageID "1999367".
- Gitelman_syndrome wikiPageRevisionID "599400719".
- Gitelman_syndrome diseasesdb "31860".
- Gitelman_syndrome emedicinesubj "article".
- Gitelman_syndrome emedicinetopic "238670".
- Gitelman_syndrome hasPhotoCollection Gitelman_syndrome.
- Gitelman_syndrome icd "N25.8 + E87.6 + E83.4".
- Gitelman_syndrome meshid "D053579".
- Gitelman_syndrome name "Gitelman syndrome".
- Gitelman_syndrome omim "263800".
- Gitelman_syndrome wordnet_type synset-disease-noun-1.
- Gitelman_syndrome subject Category:Autosomal_recessive_disorders.
- Gitelman_syndrome subject Category:Kidney_diseases.
- Gitelman_syndrome subject Category:Membrane_transport_protein_disorders.
- Gitelman_syndrome subject Category:Rare_diseases.
- Gitelman_syndrome type Abstraction100002137.
- Gitelman_syndrome type Attribute100024264.
- Gitelman_syndrome type AutosomalRecessiveDisorders.
- Gitelman_syndrome type Condition113920835.
- Gitelman_syndrome type Disease114070360.
- Gitelman_syndrome type Disorder114052403.
- Gitelman_syndrome type IllHealth114052046.
- Gitelman_syndrome type Illness114061805.
- Gitelman_syndrome type MembraneTransportProteinDisorders.
- Gitelman_syndrome type PathologicalState114051917.
- Gitelman_syndrome type PhysicalCondition114034177.
- Gitelman_syndrome type State100024720.
- Gitelman_syndrome type Disease.
- Gitelman_syndrome type AilmentCondition.
- Gitelman_syndrome type Situation.
- Gitelman_syndrome comment "Gitelman syndrome is an autosomal recessive kidney disorder characterized by hypokalemic metabolic alkalosis with hypocalciuria, and hypomagnesemia. It is caused by loss of function mutations of the thiazide sensitive sodium-chloride symporter (also known as NCC, NCCT, or TSC) located in the distal convoluted tubule.Gitelman syndrome was formerly considered a subset of Bartter syndrome until the distinct genetic and molecular bases of these disorders were identified.".
- Gitelman_syndrome label "Gitelman syndrome".
- Gitelman_syndrome label "Gitelman-Syndrom".
- Gitelman_syndrome label "Syndroom van Gitelman".
- Gitelman_syndrome label "Síndrome de Gitelman".
- Gitelman_syndrome label "Zespół Gitelmana".
- Gitelman_syndrome sameAs Gitelman-Syndrom.
- Gitelman_syndrome sameAs 지텔만_증후군.
- Gitelman_syndrome sameAs Syndroom_van_Gitelman.
- Gitelman_syndrome sameAs Zespół_Gitelmana.
- Gitelman_syndrome sameAs Síndrome_de_Gitelman.
- Gitelman_syndrome sameAs m.06c_0x.
- Gitelman_syndrome sameAs Q1053120.
- Gitelman_syndrome sameAs Q1053120.
- Gitelman_syndrome sameAs 447.
- Gitelman_syndrome sameAs Gitelman_syndrome.
- Gitelman_syndrome wasDerivedFrom Gitelman_syndrome?oldid=599400719.
- Gitelman_syndrome depiction Gitelman_syndrome.jpg.
- Gitelman_syndrome isPrimaryTopicOf Gitelman_syndrome.
- Gitelman_syndrome name "Gitelman syndrome".
