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Terminology chevron_right Concepts chevron_right 204762005

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Component

204762005

The component that hold information about this concept.

Fully Specified Name (FSN)

Transposition of cecum (disorder)

Shortest Term

Transposition of cecum

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

Transposition of cecum (disorder)

SCTID: 204762005, Defined, Active

204762005|Transposition of cecum (disorder)|

en Transposition of caecum
en Transposition of cecum
en Transposition of cecum (disorder)

Expression

204762005 |Transposition of cecum (disorder)|
 === 1492007 |Congenital anomaly of large intestine (disorder)| + 
128525008 |Disorder of cecum (disorder)| + 
39719008 |Transposition of intestine (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 56591001 |Transposition (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 32713005 |Cecum structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
313994013 - Transposition of caecum (en) View
313994013	en	Synonym (core metadata concept)	Transposition of caecum	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
313995014 - Transposition of cecum (en) View
313995014	en	Synonym (core metadata concept)	Transposition of cecum	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
590033019 - Transposition of cecum (disorder) (en) View
590033019	en	Fully specified name (core metadata concept)	Transposition of cecum (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (468924028) - 204762005 -> 56591001 (116676008) View
116676008 \|Associated morphology (attribute)\|	56591001 \|Transposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (468926026) - 204762005 -> 32713005 (363698007) View
363698007 \|Finding site (attribute)\|	32713005 \|Cecum structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4971510023) - 204762005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5017350029) - 204762005 -> 56591001 (116676008) View
116676008 \|Associated morphology (attribute)\|	56591001 \|Transposition (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5017351025) - 204762005 -> 32713005 (363698007) View
363698007 \|Finding site (attribute)\|	32713005 \|Cecum structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6109505020) - 204762005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10529647022) - 204762005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2569117023) - 204762005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3400136021) - 204762005 -> 56591001 (116676008) View
116676008 \|Associated morphology (attribute)\|	56591001 \|Transposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3400137028) - 204762005 -> 32713005 (363698007) View
363698007 \|Finding site (attribute)\|	32713005 \|Cecum structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (468927024) - 204762005 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1939203029) - 204762005 -> 1492007 (116680003) View
116680003 \|Is a (attribute)\|	1492007 \|Congenital anomaly of large intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (468925027) - 204762005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (23406024) - 204762005 -> 39719008 (116680003) View
116680003 \|Is a (attribute)\|	39719008 \|Transposition of intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (23407026) - 204762005 -> 128525008 (116680003) View
116680003 \|Is a (attribute)\|	128525008 \|Disorder of cecum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
39719008 View
39719008	Transposition of intestine (disorder)	Intestinal transposition	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1492007 View
1492007	Congenital anomaly of large intestine (disorder)	Congenital anomaly of large intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128525008 View
128525008	Disorder of cecum (disorder)	Disease of cecum	900000000000073002 \|Sufficiently defined by necessary conditions 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 (25be65fe-31d7-55c7-b679-eba4afb6217c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q43.8	TRUE	ALWAYS Q43.8	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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