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Terminology chevron_right Concepts chevron_right 79510004

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Component

79510004

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital displacement of esophagus (disorder)

Shortest Term

Congenital malpositioned esophagus

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

Congenital displacement of esophagus (disorder)

SCTID: 79510004, Primitive, Active

79510004|Congenital displacement of esophagus (disorder)|

en Congenital displacement of esophagus
en Congenital displacement of esophagus (disorder)
en Congenital displacement of oesophagus
en Congenital malpositioned esophagus
en Congenital malpositioned oesophagus
en Congenital malposition of esophagus
en Congenital malposition of oesophagus

Expression

79510004 |Congenital displacement of esophagus (disorder)|
 <<< 69771008 |Congenital anomaly of esophagus (disorder)| + 
73943003 |Congenital malposition of digestive organs (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 408737001 |Malposition (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 32849002 |Esophageal 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
131904016 - Congenital displacement of esophagus (en) View
131904016	en	Synonym (core metadata concept)	Congenital displacement of esophagus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
820568015 - Congenital displacement of esophagus (disorder) (en) View
820568015	en	Fully specified name (core metadata concept)	Congenital displacement of esophagus (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
504130013 - Congenital displacement of oesophagus (en) View
504130013	en	Synonym (core metadata concept)	Congenital displacement of oesophagus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
131906019 - Congenital malpositioned esophagus (en) View
131906019	en	Synonym (core metadata concept)	Congenital malpositioned esophagus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
200799015 - Congenital malpositioned oesophagus (en) View
200799015	en	Synonym (core metadata concept)	Congenital malpositioned oesophagus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
131905015 - Congenital malposition of esophagus (en) View
131905015	en	Synonym (core metadata concept)	Congenital malposition of esophagus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
504131012 - Congenital malposition of oesophagus (en) View
504131012	en	Synonym (core metadata concept)	Congenital malposition of oesophagus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (872524021) - 79510004 -> 60115006 (116676008) View
116676008 \|Associated morphology (attribute)\|	60115006 \|Congenital malposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11308939023) - 79510004 -> 408737001 (116676008) View
116676008 \|Associated morphology (attribute)\|	408737001 \|Malposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (872521029) - 79510004 -> 32849002 (363698007) View
363698007 \|Finding site (attribute)\|	32849002 \|Esophageal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4974808029) - 79510004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4974810027) - 79510004 -> 32849002 (363698007) View
363698007 \|Finding site (attribute)\|	32849002 \|Esophageal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5028139024) - 79510004 -> 60115006 (116676008) View
116676008 \|Associated morphology (attribute)\|	60115006 \|Congenital malposition (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6088105020) - 79510004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10515757023) - 79510004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2601945023) - 79510004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3349261022) - 79510004 -> 32849002 (363698007) View
363698007 \|Finding site (attribute)\|	32849002 \|Esophageal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3349262026) - 79510004 -> 60115006 (116676008) View
116676008 \|Associated morphology (attribute)\|	60115006 \|Congenital malposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2551275029) - 79510004 -> 73943003 (116680003) View
116680003 \|Is a (attribute)\|	73943003 \|Congenital malposition of digestive organs (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1779073025) - 79510004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1779074020) - 79510004 -> 51289009 (363698007) View
363698007 \|Finding site (attribute)\|	51289009 \|Digestive tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (872522020) - 79510004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (872523026) - 79510004 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (872525022) - 79510004 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (277291024) - 79510004 -> 69771008 (116680003) View
116680003 \|Is a (attribute)\|	69771008 \|Congenital anomaly of esophagus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
69771008 View
69771008	Congenital anomaly of esophagus (disorder)	Dị tật bẩm sinh của thực quản	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
73943003 View
73943003	Congenital malposition of digestive organs (disorder)	Congenital malposition of digestive organs	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 (7e0cbb3b-9632-540a-8261-e2f82151bed6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q39.8	TRUE	ALWAYS Q39.8	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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