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Terminology chevron_right Concepts chevron_right 29679002

Production

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Component

29679002

The component that hold information about this concept.

Fully Specified Name (FSN)

Carrier of disorder (finding)

Shortest Term

Carrier

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

Carrier of disorder (finding)

SCTID: 29679002, Primitive, Active

29679002|Carrier of disorder (finding)|

vi Người mang bệnh (phát hiện)
en Carrier
en Carrier of disease
en Carrier of disorder
en Carrier of disorder (finding)

Expression

29679002 |Carrier of disorder (finding)|
 <<< 404684003 |Clinical finding (finding)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2006389 - Người mang bệnh (phát hiện) (vi) View
2006389	vi	Synonym (core metadata concept)	Người mang bệnh (phát hiện)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
49646012 - Carrier (en) View
49646012	en	Synonym (core metadata concept)	Carrier	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1226388012 - Carrier of disease (en) View
1226388012	en	Synonym (core metadata concept)	Carrier of disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
484360016 - Carrier of disorder (en) View
484360016	en	Synonym (core metadata concept)	Carrier of disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
760599017 - Carrier of disorder (finding) (en) View
760599017	en	Fully specified name (core metadata concept)	Carrier of disorder (finding)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
49645011 - Carrier, NOS (en) View
49645011	en	Synonym (core metadata concept)	Carrier, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
49643016 - Carrier state (en) View
49643016	en	Synonym (core metadata concept)	Carrier state	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
49644010 - Carrier state, NOS (en) View
49644010	en	Synonym (core metadata concept)	Carrier state, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (196278022) - 29679002 -> 105724001 (116680003) View
116680003 \|Is a (attribute)\|	105724001 \|Disease related state (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (746247027) - 29679002 -> 278844005 (363714003) View
363714003 \|Interprets (attribute)\|	278844005 \|General clinical state (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16087995020) - 29679002 -> 404684003 (116680003) View
116680003 \|Is a (attribute)\|	404684003 \|Clinical finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
404684003 View
404684003	Clinical finding (finding)	Clinical finding	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
66871000119108 View
66871000119108	Carrier of metabolic disorder (finding)	Carrier of metabolic disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
286471000119100 View
286471000119100	Carrier of neurogenetic disorder (finding)	Carrier of neurogenetic disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
736703007 View
736703007	Carrier of hemochromatosis hfe gene mutation (finding)	Carrier of hemochromatosis hfe gene mutation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
66611000119101 View
66611000119101	Carrier of chromosome disorder (finding)	Carrier of chromosome disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
66598005 View
66598005	Carrier of infectious organism (finding)	Carrier, infectious agent	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
441520002 View
441520002	Carrier of cystic fibrosis gene mutation (finding)	Cystic fibrosis gene carrier	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
441646007 View
441646007	Carrier of tay sachs disease gene mutation (finding)	Mang gen bệnh tay sachs (phát hiện)	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
442018007 View
442018007	Carrier of sickle cell gene mutation (finding)	Carrier of sickle cell gene mutation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
24800002 View
24800002	Carrier state, disease not expressed (finding)	Carrier, disease not expressed	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
47461006 View
47461006	Genetic disorder carrier (finding)	Genetic disorder carrier	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
87955000 View
87955000	Carrier state, disease expressed (finding)	Carrier, disease expressed	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
191301000 View
191301000	Hemophilia carrier (finding)	Hemophilia carrier	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (902494c9-1b07-5f51-929e-5f3899ee291a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

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