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Terminology chevron_right Concepts chevron_right 128332003

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Component

128332003

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of digestive organ (disorder)

Shortest Term

Congenital anomaly of digestive organ

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 organ (disorder)

SCTID: 128332003, Defined, Active

128332003|Congenital anomaly of digestive organ (disorder)|

en Congenital anomaly of digestive organ
en Congenital anomaly of digestive organ (disorder)
en Congenital malformation of digestive organ

Expression

128332003 |Congenital anomaly of digestive organ (disorder)|
 === 76712006 |Disorder of digestive organ (disorder)| + 
69518005 |Congenital anomaly of digestive system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 49596003 |Digestive organ 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
206621012 - Congenital anomaly of digestive organ (en) View
206621012	en	Synonym (core metadata concept)	Congenital anomaly of digestive organ	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
732311019 - Congenital anomaly of digestive organ (disorder) (en) View
732311019	en	Fully specified name (core metadata concept)	Congenital anomaly of digestive organ (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3008658011 - Congenital malformation of digestive organ (en) View
3008658011	en	Synonym (core metadata concept)	Congenital malformation of digestive organ	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (697452029) - 128332003 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4988648023) - 128332003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4988649026) - 128332003 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4988650026) - 128332003 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6096916024) - 128332003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518961022) - 128332003 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518962026) - 128332003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3366367028) - 128332003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3366368022) - 128332003 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1756421022) - 128332003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2590533025) - 128332003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (697453023) - 128332003 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1756420023) - 128332003 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (697451020) - 128332003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (163553024) - 128332003 -> 76712006 (116680003) View
116680003 \|Is a (attribute)\|	76712006 \|Disorder of digestive organ (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (163554029) - 128332003 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
69518005 View
69518005	Congenital anomaly of digestive system (disorder)	Congenital anomaly of digestive system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
76712006 View
76712006	Disorder of digestive organ (disorder)	Disease of digestive organ	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
86595004 View
86595004	Congenital mesocolic hernia (disorder)	Congenital mesocolic hernia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
10883005 View
10883005	Gingival cyst of adult (disorder)	Gingival cyst of adult	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
253802003 View
253802003	Congenital mesenteric cyst (disorder)	Congenital mesenteric cyst	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
414342007 View
414342007	Gingival cyst of neonate (disorder)	Neonatal gingival cyst	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
268213006 View
268213006	Congenital abnormality of liver and/or biliary tract (disorder)	Liver and biliary system anomalies	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
445306000 View
445306000	Cleft of alveolar ridge (disorder)	Cleft of alveolar ridge	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
235977001 View
235977001	Congenital malformation of pancreas (disorder)	Dị tật bẩm sinh tuyến tụy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
422977003 View
422977003	Congenital anomaly of tooth (disorder)	Congenital anomaly of tooth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
360522009 View
360522009	Congenital epulis of newborn (disorder)	Neonatal congenital epulis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
253755003 View
253755003	Congenital malformation of salivary glands and ducts (disorder)	Congenital anomaly of salivary glands and ducts	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
389273002 View
389273002	Cherubism with gingival fibromatosis (disorder)	Ramon syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
126764002 View
126764002	Congenital anomaly of intestinal tract (disorder)	Congenital anomaly of intestinal tract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11223009 View
11223009	Congenital anomaly of pharynx (disorder)	Dị tật bẩm sinh hầu họng	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
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
40158001 View
40158001	Papillon-lefèvre syndrome (disorder)	Papillon-lefevre syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
60447007 View
60447007	Congenital anomaly of tongue (disorder)	Congenital anomaly of tongue	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
68539005 View
68539005	Congenital bronchopulmonary foregut malformation (disorder)	Dị tật phế quản phổi bẩm sinh	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
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
109520000 View
109520000	Congenital alveolar hyperplasia of mandible (disorder)	Congenital mandibular alveolar hyperplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
109521001 View
109521001	Congenital alveolar hyperplasia of maxilla (disorder)	Congenital maxillary alveolar hyperplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
109526006 View
109526006	Congenital alveolar hypoplasia of mandible (disorder)	Congenital mandibular alveolar hypoplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
109527002 View
109527002	Congenital alveolar hypoplasia of maxilla (disorder)	Congenital maxillary alveolar hypoplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
109552000 View
109552000	Buccal bifurcation cyst (disorder)	Buccal bifurcation cyst	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
123662000 View
123662000	Persistent dorsal mesentery (disorder)	Persistent common mesentery	900000000000073002 \|Sufficiently defined by necessary conditions 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 (096d765c-7461-53e3-9049-693f3f6e264e) 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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