22774003: Hypokalemic alkalosis (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Metabolic disease\...

\Disorder of fluid AND/OR electrolyte\Disorder of electrolytes\Potassium disorder\Hypokalemia\Hypokalemic alkalosis

\Disorder of acid-base balance\Alkalosis\Metabolic alkalosis\Hypokalemic alkalosis

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

38228016 Hypokalemic alkalosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

38229012 Hypokalaemic alkalosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

752219014 Hypokalemic alkalosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3422381000005114 hypokaliæmisk alkalose da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hypokalemic alkalosis	Is a	Metabolic alkalosis	true	Inferred relationship	Some
Hypokalemic alkalosis	Is a	Hypokalemia	true	Inferred relationship	Some
Hypokalemic alkalosis	Finding site	Body system structure	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial hypokalemic alkalosis, Gullner type	Is a	True	Hypokalemic alkalosis	Inferred relationship	Some
Familial hypokalemic and hypomagnesemic tubulopathy	Is a	False	Hypokalemic alkalosis	Inferred relationship	Some
Bartter syndrome (disorder)	Is a	True	Hypokalemic alkalosis	Inferred relationship	Some
Pseudoprimary hyperaldosteronism (disorder)	Is a	False	Hypokalemic alkalosis	Inferred relationship	Some
Hypokalemic alkalosis due to diarrhea	Is a	True	Hypokalemic alkalosis	Inferred relationship	Some
A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. The disease presents mainly in adolescents and adults but also encountered in children, as early as in the neonatal period. Caused by biallelic inactivating mutations in the SLC12A3 gene encoding the thiazide-sensitive sodium-chloride cotransporter NCC expressed in the apical membrane of cells lining the distal convoluted tubule. More than 350 different NCC mutations throughout the whole protein have been identified.	Is a	True	Hypokalemic alkalosis	Inferred relationship	Some

This concept is not in any reference sets