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Terminology chevron_right Concepts chevron_right 13568007

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Component

13568007

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital duplication of stomach (disorder)

Shortest Term

Duplication of stomach

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 duplication of stomach (disorder)

SCTID: 13568007, Defined, Active

13568007|Congenital duplication of stomach (disorder)|

en Congenital duplication of stomach
en Congenital duplication of stomach (disorder)
en Duplication of stomach

Expression

13568007 |Congenital duplication of stomach (disorder)|
 === 33257003 |Congenital duplication of digestive organs (disorder)| + 
60699003 |Congenital anomaly of stomach (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 18295000 |Double structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 69695003 |Stomach 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
23162018 - Congenital duplication of stomach (en) View
23162018	en	Synonym (core metadata concept)	Congenital duplication of stomach	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
738935012 - Congenital duplication of stomach (disorder) (en) View
738935012	en	Fully specified name (core metadata concept)	Congenital duplication of stomach (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
475370015 - Duplication of stomach (en) View
475370015	en	Synonym (core metadata concept)	Duplication of stomach	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4989634025) - 13568007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989636028) - 13568007 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5018341028) - 13568007 -> 18295000 (116676008) View
116676008 \|Associated morphology (attribute)\|	18295000 \|Double structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5858639026) - 13568007 -> 18295000 (116676008) View
116676008 \|Associated morphology (attribute)\|	18295000 \|Double structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5858640029) - 13568007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5858641025) - 13568007 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10527495027) - 13568007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2590790028) - 13568007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3172070024) - 13568007 -> 128347007 (116680003) View
116680003 \|Is a (attribute)\|	128347007 \|Congenital anomaly of gastrointestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3178935025) - 13568007 -> 363024001 (116680003) View
116680003 \|Is a (attribute)\|	363024001 \|Congenital anomaly of abdomen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3442153021) - 13568007 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3466475023) - 13568007 -> 18295000 (116676008) View
116676008 \|Associated morphology (attribute)\|	18295000 \|Double structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3771559029) - 13568007 -> 275262008 (116680003) View
116680003 \|Is a (attribute)\|	275262008 \|Congenital malformation of upper alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3181326028) - 13568007 -> 363026004 (116680003) View
116680003 \|Is a (attribute)\|	363026004 \|Congenital anomaly of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (701112026) - 13568007 -> 18295000 (116676008) View
116676008 \|Associated morphology (attribute)\|	18295000 \|Double structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (701115029) - 13568007 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (701111022) - 13568007 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1015704027) - 13568007 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (701113020) - 13568007 -> 18295000 (116676008) View
116676008 \|Associated morphology (attribute)\|	18295000 \|Double structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (701114025) - 13568007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (166714022) - 13568007 -> 33257003 (116680003) View
116680003 \|Is a (attribute)\|	33257003 \|Congenital duplication of digestive organs (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (166715023) - 13568007 -> 60699003 (116680003) View
116680003 \|Is a (attribute)\|	60699003 \|Congenital anomaly of stomach (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
33257003 View
33257003	Congenital duplication of digestive organs (disorder)	Congenital duplication of digestive organs	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60699003 View
60699003	Congenital anomaly of stomach (disorder)	Congenital anomaly of stomach	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 (22bc7758-707b-5cc1-ad9a-220f9f2549c7) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q40.2	TRUE	ALWAYS Q40.2	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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