721172000: Hypomagnesemia co-occurrent with normocalciuria (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Hypomagnesemia co-occurrent with normocalciuria (disorder)

\Metabolic disease\Metabolic disorder of transport (disorder)\Primary hypomagnesemia\Hypomagnesemia co-occurrent with normocalciuria (disorder)
\Metabolic disease\Disorder of fluid AND/OR electrolyte\Disorder of electrolytes\Magnesium disorder (disorder)\Hypomagnesaemia\Primary hypomagnesemia\Hypomagnesemia co-occurrent 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

3324518018 Hypomagnesemia co-occurrent with normocalciuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3324519014 Hypomagnesemia co-occurrent with normocalciuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3324520015 Hypomagnesaemia with normocalciuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3324521016 Hypomagnesemia with normocalciuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3780924012 Hypomagnesaemia co-occurrent with normocalciuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3324518018 Hypomagnesemia co-occurrent with normocalciuria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3324518018 Hypomagnesemia co-occurrent with normocalciuria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3324519014 Hypomagnesemia co-occurrent with normocalciuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3324519014 Hypomagnesemia co-occurrent with normocalciuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3324520015 Hypomagnesaemia with normocalciuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3324520015 Hypomagnesaemia with normocalciuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3324521016 Hypomagnesemia with normocalciuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3324521016 Hypomagnesemia with normocalciuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3780924012 Hypomagnesaemia co-occurrent with normocalciuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

6295741000241117 hypomagnésémie concomitante d'une normocalciurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6295751000241119 hypomagnésémie concomitante d'une calciurie normale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6295741000241117 hypomagnésémie concomitante d'une normocalciurie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6295751000241119 hypomagnésémie concomitante d'une calciurie normale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hypomagnesemia co-occurrent with normocalciuria (disorder)	Is a	Autosomal hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypomagnesemia co-occurrent with normocalciuria (disorder)	Is a	Primary hypomagnesemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets