717788000: familiaire primaire hypomagnesiëmie met normocalciurie (aandoening)

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

6024511000146113 familiaire primaire hypomagnesiëmie met normocalciurie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6024521000146115 familiaire primaire hypomagnesiëmie met normocalciurie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6024531000146118 familiale primaire hypomagnesiëmie met normocalciurie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial primary hypomagnesemia with normocalciuria (disorder)	Is a	Autosomal hereditary disorder	true	Inferred relationship	Some
Familial primary hypomagnesemia with normocalciuria (disorder)	Is a	Primary hypomagnesemia	true	Inferred relationship	Some
Familial primary hypomagnesemia with normocalciuria (disorder)	Is a	Hereditary metabolic disease	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Familial primary hypomagnesemia with normocalciuria and normocalcemia (disorder)	Is a	True	Familial primary hypomagnesemia with normocalciuria (disorder)	Inferred relationship	Some

This concept is not in any reference sets