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Terminology chevron_right Concepts chevron_right 53076002

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Component

53076002

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital gastric perforation (disorder)

Shortest Term

Neonatal gastric perforation

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 gastric perforation (disorder)

SCTID: 53076002, Defined, Active

53076002|Congenital gastric perforation (disorder)|

en Congenital gastric perforation
en Congenital gastric perforation (disorder)
en Neonatal gastric perforation

Expression

53076002 |Congenital gastric perforation (disorder)|
 === 60699003 |Congenital anomaly of stomach (disorder)| + 
235674005 |Perforation of stomach (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 36191001 |Perforation (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
88291017 - Congenital gastric perforation (en) View
88291017	en	Synonym (core metadata concept)	Congenital gastric perforation	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
791155019 - Congenital gastric perforation (disorder) (en) View
791155019	en	Fully specified name (core metadata concept)	Congenital gastric perforation (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
88292012 - Neonatal gastric perforation (en) View
88292012	en	Synonym (core metadata concept)	Neonatal gastric perforation	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (804700024) - 53076002 -> 88890009 (116676008) View
116676008 \|Associated morphology (attribute)\|	88890009 \|Congenital perforation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11300965023) - 53076002 -> 36191001 (116676008) View
116676008 \|Associated morphology (attribute)\|	36191001 \|Perforation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (804703021) - 53076002 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6033903026) - 53076002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6033904021) - 53076002 -> 88890009 (116676008) View
116676008 \|Associated morphology (attribute)\|	88890009 \|Congenital perforation (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6033905022) - 53076002 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6078644023) - 53076002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517619027) - 53076002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3417570020) - 53076002 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3444745023) - 53076002 -> 88890009 (116676008) View
116676008 \|Associated morphology (attribute)\|	88890009 \|Congenital perforation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4987217023) - 53076002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4987218029) - 53076002 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4987219021) - 53076002 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2597588028) - 53076002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3172087021) - 53076002 -> 128347007 (116680003) View
116680003 \|Is a (attribute)\|	128347007 \|Congenital anomaly of gastrointestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3179250024) - 53076002 -> 363024001 (116680003) View
116680003 \|Is a (attribute)\|	363024001 \|Congenital anomaly of abdomen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3772774027) - 53076002 -> 275262008 (116680003) View
116680003 \|Is a (attribute)\|	275262008 \|Congenital malformation of upper alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3180982029) - 53076002 -> 363026004 (116680003) View
116680003 \|Is a (attribute)\|	363026004 \|Congenital anomaly of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (804699023) - 53076002 -> 36191001 (116676008) View
116676008 \|Associated morphology (attribute)\|	36191001 \|Perforation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2548326026) - 53076002 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3772773022) - 53076002 -> 235674005 (116680003) View
116680003 \|Is a (attribute)\|	235674005 \|Perforation of stomach (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (804698026) - 53076002 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (804701023) - 53076002 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1770263029) - 53076002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1770264024) - 53076002 -> 51289009 (363698007) View
363698007 \|Finding site (attribute)\|	51289009 \|Digestive tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (804702027) - 53076002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (234413022) - 53076002 -> 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
235674005 View
235674005	Perforation of stomach (disorder)	Perforation of stomach	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 (ff19195c-0a6d-526c-889d-ee6d9f36e121) 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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