722008003: Isolated autosomal dominant hypomagnesemia Glaudemans type (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Isolated autosomal dominant hypomagnesemia Glaudemans type
• \Metabolic disease\Metabolic disorder of transport\Primary hypomagnesemia\Isolated autosomal dominant hypomagnesemia Glaudemans type
• \Metabolic disease\Disorder of fluid AND/OR electrolyte\Disorder of electrolytes\Magnesium disorder\Hypomagnesemia\Primary hypomagnesemia\Isolated autosomal dominant hypomagnesemia Glaudemans type

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3313725017	Isolated autosomal dominant hypomagnesemia Glaudemans type (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3313735011	Isolated autosomal dominant hypomagnesemia Glaudemans type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3330121010	Isolated autosomal dominant hypomagnesaemia Glaudemans type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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