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Terminology chevron_right Concepts chevron_right 286471000119100

Production

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Language with ID “f2ce0d77-d1d4-5d99-b880-4757f4d23a11” doesn’t exist. Perhaps it was deleted?

Component

286471000119100

The component that hold information about this concept.

Fully Specified Name (FSN)

Carrier of neurogenetic disorder (finding)

Shortest Term

Carrier of neurogenetic disorder

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 neurogenetic disorder (finding)

SCTID: 286471000119100, Primitive, Active

286471000119100|Carrier of neurogenetic disorder (finding)|

vi Người mang bệnh thần kinh di truyền (phát hiện)
en Carrier of neurogenetic disorder
en Carrier of neurogenetic disorder (finding)

Expression

286471000119100 |Carrier of neurogenetic disorder (finding)|
 <<< 29679002 |Carrier of disorder (finding)| : 
        { 363714003 |Interprets (attribute)| = 278844005 |General clinical state (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2006422 - Người mang bệnh thần kinh di truyền (phát hiện) (vi) View
2006422	vi	Synonym (core metadata concept)	Người mang bệnh thần kinh di truyền (phát hiện)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5259845011 - Carrier of neurogenetic disorder (en) View
5259845011	en	Synonym (core metadata concept)	Carrier of neurogenetic disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5259844010 - Carrier of neurogenetic disorder (finding) (en) View
5259844010	en	Fully specified name (core metadata concept)	Carrier of neurogenetic disorder (finding)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16088000020) - 286471000119100 -> 365860008 (116680003) View
116680003 \|Is a (attribute)\|	365860008 \|General clinical state finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15726434025) - 286471000119100 -> 29679002 (116680003) View
116680003 \|Is a (attribute)\|	29679002 \|Carrier of disorder (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15726435029) - 286471000119100 -> 278844005 (363714003) View
363714003 \|Interprets (attribute)\|	278844005 \|General clinical state (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
29679002 View
29679002	Carrier of disorder (finding)	Carrier	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 (9cae8920-705b-59a5-bd6a-d6e53a80efcc) 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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