717788000: hypomagnésémie primaire familiale avec normocalcurie (trouble)

• SNOMED CT Concept\constatation clinique\Disease\...
• \Genetic disease\maladie héréditaire\Autosomal hereditary disorder\hypomagnésémie primaire familiale avec normocalcurie
• \trouble métabolique\trouble métabolique du transport\Primary hypomagnesemia\hypomagnésémie primaire familiale avec normocalcurie
• \trouble métabolique\déséquilibre hydroelectrolytique\Disorder of electrolytes\Magnesium disorder (disorder)\hypomagnésémie\Primary hypomagnesemia\hypomagnésémie primaire familiale avec normocalcurie

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
1002081000172117	hypomagnésémie primaire familiale avec normocalcurie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
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
751521000241117	hypomagnésémie primaire familiale avec normocalcurie (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

Back to Start