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Terminology chevron_right Concepts chevron_right 445554007

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Component

445554007

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital asymmetry of tonsils (disorder)

Shortest Term

Bất đối xứng amidan bẩm sinh

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Congenital asymmetry of tonsils (disorder)

SCTID: 445554007, Defined, Active

445554007|Congenital asymmetry of tonsils (disorder)|

vi Bất đối xứng amidan bẩm sinh
en Congenital asymmetry of tonsils
en Congenital asymmetry of tonsils (disorder)

Expression

445554007 |Congenital asymmetry of tonsils (disorder)|
 === 306962003 |Tonsil asymmetry (finding)| + 
87290003 |Congenital anomaly of head (disorder)| + 
11223009 |Congenital anomaly of pharynx (disorder)| + 
40888008 |Congenital anomaly of the hematopoietic system (disorder)| + 
23023009 |Disorder of palatine tonsil (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 5804003 |Congenital growth disproportion (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 75573002 |Palatine tonsillar structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363714003 |Interprets (attribute)| = 364046004 |Appearance of tonsil (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
536161000003111 - bất đối xứng amidan bẩm sinh (vi) View
536161000003111	vi	Synonym (core metadata concept)	bất đối xứng amidan bẩm sinh	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
2871850013 - Congenital asymmetry of tonsils (en) View
2871850013	en	Synonym (core metadata concept)	Congenital asymmetry of tonsils	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2868897015 - Congenital asymmetry of tonsils (disorder) (en) View
2868897015	en	Fully specified name (core metadata concept)	Congenital asymmetry of tonsils (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15508304022) - 445554007 -> 364046004 (363714003) View
363714003 \|Interprets (attribute)\|	364046004 \|Appearance of tonsil (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6024305025) - 445554007 -> 363027008 (116680003) View
116680003 \|Is a (attribute)\|	363027008 \|Congenital anomaly of body wall (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10514332020) - 445554007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6024304026) - 445554007 -> 87290003 (116680003) View
116680003 \|Is a (attribute)\|	87290003 \|Congenital anomaly of head (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6024306029) - 445554007 -> 11223009 (116680003) View
116680003 \|Is a (attribute)\|	11223009 \|Congenital anomaly of pharynx (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6024307022) - 445554007 -> 40888008 (116680003) View
116680003 \|Is a (attribute)\|	40888008 \|Congenital anomaly of the hematopoietic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6024308028) - 445554007 -> 23023009 (116680003) View
116680003 \|Is a (attribute)\|	23023009 \|Disorder of palatine tonsil (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3775354027) - 445554007 -> 23023009 (116680003) View
116680003 \|Is a (attribute)\|	23023009 \|Disorder of palatine tonsil (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3775356025) - 445554007 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3778689021) - 445554007 -> 75573002 (363698007) View
363698007 \|Finding site (attribute)\|	75573002 \|Palatine tonsillar structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3778690028) - 445554007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4979577025) - 445554007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4979578024) - 445554007 -> 75573002 (363698007) View
363698007 \|Finding site (attribute)\|	75573002 \|Palatine tonsillar structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5008187023) - 445554007 -> 5804003 (116676008) View
116676008 \|Associated morphology (attribute)\|	5804003 \|Congenital growth disproportion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3775355026) - 445554007 -> 306962003 (116680003) View
116680003 \|Is a (attribute)\|	306962003 \|Tonsil asymmetry (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
11223009 View
11223009	Congenital anomaly of pharynx (disorder)	Dị tật bẩm sinh hầu họng	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
23023009 View
23023009	Disorder of palatine tonsil (disorder)	Disorder of tonsil	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
40888008 View
40888008	Congenital anomaly of the hematopoietic system (disorder)	Congenital anomaly of the hematopoietic system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
87290003 View
87290003	Congenital anomaly of head (disorder)	Congenital anomaly of head	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
306962003 View
306962003	Tonsil asymmetry (finding)	Tonsil asymmetry	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 (894d2692-7bfb-5467-8f2e-00a661b68367) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q40.8	TRUE	ALWAYS Q40.8	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)\|
ExtendedMap object (bfce6f0c-6982-52fc-9052-305c60a417a8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q38.8	TRUE	ALWAYS Q38.8	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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