725031005: Familial primary hypomagnesemia with normocalciuria and normocalcemia (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3437074019	Familial primary hypomagnesemia with normocalciuria and normocalcemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3437075018	Familial primary hypomagnesemia with normocalciuria and normocalcemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3437076017	Familial primary hypomagnesaemia with normocalciuria and normocalcemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3437077014	FPHNN - familial primary hypomagnesemia with normocalciuria and normocalcemia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3437078016	FPHNN - familial primary hypomagnesaemia with normocalciuria and normocalcemia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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