717788000: Familial primary hypomagnesemia with normocalciuria (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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	Entire term case insensitive (core metadata concept)	SNOMED CT core
3310272017	Familial primary hypomagnesemia with normocalciuria	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3311715019	Familial primary hypomagnesaemia with normocalciuria	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3896651000052116	familjär primär hypomagnesemi med normokalciuri	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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