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Terminology chevron_right Concepts chevron_right 48655003

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Component

48655003

The component that hold information about this concept.

Fully Specified Name (FSN)

Isolated familial renal hypomagnesemia (disorder)

Shortest Term

Isolated familial renal hypomagnesemia

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Isolated familial renal hypomagnesemia (disorder)

SCTID: 48655003, Primitive, Active

48655003|Isolated familial renal hypomagnesemia (disorder)|

en Isolated familial renal hypomagnesaemia
en Isolated familial renal hypomagnesemia
en Isolated familial renal hypomagnesemia (disorder)

Expression

48655003 |Isolated familial renal hypomagnesemia (disorder)|
 <<< 80710001 |Primary hypomagnesemia (disorder)| + 
111941005 |Familial disease (disorder)| + 
782964007 |Genetic disease (disorder)| + 
106000008 |Metabolic renal disease (disorder)| : 
        { 363698007 |Finding site (attribute)| = 64033007 |Kidney structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
495167015 - Isolated familial renal hypomagnesaemia (en) View
495167015	en	Synonym (core metadata concept)	Isolated familial renal hypomagnesaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
81069013 - Isolated familial renal hypomagnesemia (en) View
81069013	en	Synonym (core metadata concept)	Isolated familial renal hypomagnesemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
786247019 - Isolated familial renal hypomagnesemia (disorder) (en) View
786247019	en	Fully specified name (core metadata concept)	Isolated familial renal hypomagnesemia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (227238025) - 48655003 -> 90708001 (116680003) View
116680003 \|Is a (attribute)\|	90708001 \|Kidney disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15058019029) - 48655003 -> 106000008 (116680003) View
116680003 \|Is a (attribute)\|	106000008 \|Metabolic renal disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1676406027) - 48655003 -> 236526008 (116680003) View
116680003 \|Is a (attribute)\|	236526008 \|Renal disorders in inherited disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12251959024) - 48655003 -> 111941005 (116680003) View
116680003 \|Is a (attribute)\|	111941005 \|Familial disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251960025) - 48655003 -> 782964007 (116680003) View
116680003 \|Is a (attribute)\|	782964007 \|Genetic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (793741020) - 48655003 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (227237024) - 48655003 -> 80710001 (116680003) View
116680003 \|Is a (attribute)\|	80710001 \|Primary hypomagnesemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
106000008 View
106000008	Metabolic renal disease (disorder)	Metabolic renal disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
782964007 View
782964007	Genetic disease (disorder)	Genetic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
80710001 View
80710001	Primary hypomagnesemia (disorder)	Primary hypomagnesemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
111941005 View
111941005	Familial disease (disorder)	Familial disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (8c545244-4767-534b-9337-2f81ed96ce68) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.4	TRUE	ALWAYS E83.4	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

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