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Terminology chevron_right Concepts chevron_right 69518005

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Component

69518005

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of digestive system (disorder)

Shortest Term

Congenital anomaly of digestive system

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 anomaly of digestive system (disorder)

SCTID: 69518005, Defined, Active

69518005|Congenital anomaly of digestive system (disorder)|

en Congenital anomaly of digestive system
en Congenital anomaly of digestive system (disorder)
en Congenital deformity of digestive system
en Congenital malformation of the digestive system

Expression

69518005 |Congenital anomaly of digestive system (disorder)|
 === 276654001 |Congenital malformation (disorder)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 86762007 |Structure of digestive system (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
115500015 - Congenital anomaly of digestive system (en) View
115500015	en	Synonym (core metadata concept)	Congenital anomaly of digestive system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
809472015 - Congenital anomaly of digestive system (disorder) (en) View
809472015	en	Fully specified name (core metadata concept)	Congenital anomaly of digestive system (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
115503018 - Congenital deformity of digestive system (en) View
115503018	en	Synonym (core metadata concept)	Congenital deformity of digestive system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
501310018 - Congenital malformation of the digestive system (en) View
501310018	en	Synonym (core metadata concept)	Congenital malformation of the digestive system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
115504012 - Congenital alimentary tract anomaly, NOS (en) View
115504012	en	Synonym (core metadata concept)	Congenital alimentary tract anomaly, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
115501016 - Congenital anomaly of digestive system, NOS (en) View
115501016	en	Synonym (core metadata concept)	Congenital anomaly of digestive system, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
115502011 - Congenital deformity of digestive system, NOS (en) View
115502011	en	Synonym (core metadata concept)	Congenital deformity of digestive system, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (261143022) - 69518005 -> 53619000 (116680003) View
116680003 \|Is a (attribute)\|	53619000 \|Disorder of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15880824028) - 69518005 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (847344029) - 69518005 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5017521024) - 69518005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5017522028) - 69518005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5017523022) - 69518005 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6084503025) - 69518005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10524314021) - 69518005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10524315022) - 69518005 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3408534029) - 69518005 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3445609023) - 69518005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5020231029) - 69518005 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1775871023) - 69518005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2550131025) - 69518005 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2600264025) - 69518005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (261144027) - 69518005 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (847345028) - 69518005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
276654001 View
276654001	Congenital malformation (disorder)	Dị tật bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
95471008 View
95471008	Congenital arteriovenous malformation of gastrointestinal tract (disorder)	Congenital arteriovenous anomaly of gastrointestinal tract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95470009 View
95470009	Congenital anomaly of digestive tract (disorder)	Congenital digestive tract anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128332003 View
128332003	Congenital anomaly of digestive organ (disorder)	Congenital anomaly of digestive organ	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
302961007 View
302961007	Hereditary splenic hypoplasia (disorder)	Hereditary splenic hypoplasia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (ccea0737-e2dd-5e2f-b98a-eb35a72084ac) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q45.9	TRUE	ALWAYS Q45.9	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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