721172000: Hypomagnesemia co-occurrent with normocalciuria (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hypomagnesaemia co-occurrent with normocalciuria
• \Metabolic disease\Metabolic disorder of transport\Primary hypomagnesaemia\Hypomagnesaemia co-occurrent with normocalciuria
• \Metabolic disease\Disorder of fluid AND/OR electrolyte\Disorder of electrolytes\Magnesium disorder\Hypomagnesaemia\Primary hypomagnesaemia\Hypomagnesaemia co-occurrent with normocalciuria

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3324518018	Hypomagnesemia co-occurrent with normocalciuria (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3324519014	Hypomagnesemia co-occurrent with normocalciuria	en	Synonym	Active	Case insensitive	SNOMED CT core
3324520015	Hypomagnesaemia with normocalciuria	en	Synonym	Active	Case insensitive	SNOMED CT core
3324521016	Hypomagnesemia with normocalciuria	en	Synonym	Active	Case insensitive	SNOMED CT core
3780924012	Hypomagnesaemia co-occurrent with normocalciuria	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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