717788000: Familial primary hypomagnesemia with normocalciuria (disorder)

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

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3310271012	Familial primary hypomagnesemia with normocalciuria (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3310272017	Familial primary hypomagnesemia with normocalciuria	en	Synonym	Active	Case insensitive	SNOMED CT core
3311715019	Familial primary hypomagnesaemia 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

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