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Terminology chevron_right Concepts chevron_right 105992002

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Component

105992002

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of tongue, salivary gland and/or pharynx (disorder)

Shortest Term

Congenital anomaly of tongue, salivary gland and/or pharynx

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 anomaly of tongue, salivary gland and/or pharynx (disorder)

SCTID: 105992002, Primitive, Active

105992002|Congenital anomaly of tongue, salivary gland and/or pharynx (disorder)|

en Congenital anomaly of tongue, salivary gland and/or pharynx
en Congenital anomaly of tongue, salivary gland and/or pharynx (disorder)

Expression

105992002 |Congenital anomaly of tongue, salivary gland and/or pharynx (disorder)|
 <<< 275262008 |Congenital malformation of upper alimentary tract (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 127868003 |Upper digestive tract 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
170411010 - Congenital anomaly of tongue, salivary gland AND/OR pharynx (en) View
170411010	en	Synonym (core metadata concept)	Congenital anomaly of tongue, salivary gland AND/OR pharynx	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
577017014 - Congenital anomaly of tongue, salivary gland AND/OR pharynx (disorder) (en) View
577017014	en	Fully specified name (core metadata concept)	Congenital anomaly of tongue, salivary gland AND/OR pharynx (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3441917021) - 105992002 -> 127868003 (363698007) View
363698007 \|Finding site (attribute)\|	127868003 \|Upper digestive tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4975753026) - 105992002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4975755022) - 105992002 -> 127868003 (363698007) View
363698007 \|Finding site (attribute)\|	127868003 \|Upper digestive tract structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4986268025) - 105992002 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6094307026) - 105992002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10523178027) - 105992002 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10523179024) - 105992002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (19758020) - 105992002 -> 34588007 (116680003) View
116680003 \|Is a (attribute)\|	34588007 \|Congenital anomaly of upper alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2568568020) - 105992002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3355217025) - 105992002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3618581025) - 105992002 -> 443341004 (116680003) View
116680003 \|Is a (attribute)\|	443341004 \|Congenital anomaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5019650028) - 105992002 -> 275262008 (116680003) View
116680003 \|Is a (attribute)\|	275262008 \|Congenital malformation of upper alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1720687024) - 105992002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2777790023) - 105992002 -> 127868003 (363698007) View
363698007 \|Finding site (attribute)\|	127868003 \|Upper digestive tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3181315023) - 105992002 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (463016022) - 105992002 -> 62834003 (363698007) View
363698007 \|Finding site (attribute)\|	62834003 \|Upper gastrointestinal tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2690141023) - 105992002 -> 128347007 (116680003) View
116680003 \|Is a (attribute)\|	128347007 \|Congenital anomaly of gastrointestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2690142027) - 105992002 -> 119291004 (116680003) View
116680003 \|Is a (attribute)\|	119291004 \|Disorder of upper gastrointestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1720686026) - 105992002 -> 51289009 (363698007) View
363698007 \|Finding site (attribute)\|	51289009 \|Digestive tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (463015021) - 105992002 -> 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
275262008 View
275262008	Congenital malformation of upper alimentary tract (disorder)	Congenital anomaly of upper digestive tract	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 (8e17167a-ad7a-5982-b0e2-ab43595a95a9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

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