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Terminology chevron_right Concepts chevron_right 60876000

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Component

60876000

The component that hold information about this concept.

Fully Specified Name (FSN)

Gardner syndrome (disorder)

Shortest Term

Gardner syndrome

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

Gardner syndrome (disorder)

SCTID: 60876000, Primitive, Active

60876000|Gardner syndrome (disorder)|

en Gardner syndrome (disorder)
en Gs - gardner's syndrome
en Gardner syndrome

Expression

60876000 |Gardner syndrome (disorder)|
 <<< 363070008 |Developmental hereditary disorder (disorder)| + 
399960008 |Congenital hamartoma (disorder)| + 
1492007 |Congenital anomaly of large intestine (disorder)| + 
254594009 |Hamartoma of intestine (disorder)| + 
72900001 |Familial multiple polyposis syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 9499001 |Multiple polyps (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 14742008 |Large intestinal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 51398009 |Hamartoma (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 14742008 |Large intestinal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
799876013 - Gardner syndrome (disorder) (en) View
799876013	en	Fully specified name (core metadata concept)	Gardner syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
1232143012 - GS - Gardner's syndrome (en) View
1232143012	en	Synonym (core metadata concept)	GS - Gardner's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
101150018 - Gardner syndrome (en) View
101150018	en	Synonym (core metadata concept)	Gardner syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10525206024) - 60876000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13068898024) - 60876000 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12085606020) - 60876000 -> 254594009 (116680003) View
116680003 \|Is a (attribute)\|	254594009 \|Hamartoma of intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12085607027) - 60876000 -> 14742008 (363698007) View
363698007 \|Finding site (attribute)\|	14742008 \|Large intestinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10525203027) - 60876000 -> 1492007 (116680003) View
116680003 \|Is a (attribute)\|	1492007 \|Congenital anomaly of large intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10525204022) - 60876000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10525205023) - 60876000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1678893029) - 60876000 -> 281867008 (116680003) View
116680003 \|Is a (attribute)\|	281867008 \|Multisystem disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (247145025) - 60876000 -> 75523000 (116680003) View
116680003 \|Is a (attribute)\|	75523000 \|Congenital hamartosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (825644028) - 60876000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268556024) - 60876000 -> 51398009 (116676008) View
116676008 \|Associated morphology (attribute)\|	51398009 \|Hamartoma (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010261022) - 60876000 -> 399960008 (116680003) View
116680003 \|Is a (attribute)\|	399960008 \|Congenital hamartoma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5010262026) - 60876000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5010263020) - 60876000 -> 51398009 (116676008) View
116676008 \|Associated morphology (attribute)\|	51398009 \|Hamartoma (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2268557026) - 60876000 -> 108369006 (116676008) View
116676008 \|Associated morphology (attribute)\|	108369006 \|Neoplasm (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (825642029) - 60876000 -> 14742008 (363698007) View
363698007 \|Finding site (attribute)\|	14742008 \|Large intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (825643023) - 60876000 -> 9499001 (116676008) View
116676008 \|Associated morphology (attribute)\|	9499001 \|Multiple polyps (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3421727028) - 60876000 -> 9499001 (116676008) View
116676008 \|Associated morphology (attribute)\|	9499001 \|Multiple polyps (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3460976023) - 60876000 -> 14742008 (363698007) View
363698007 \|Finding site (attribute)\|	14742008 \|Large intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2268555023) - 60876000 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268558020) - 60876000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1772848025) - 60876000 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (247142027) - 60876000 -> 312568001 (116680003) View
116680003 \|Is a (attribute)\|	312568001 \|Multisystem disorder g-h (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (247143021) - 60876000 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (247144026) - 60876000 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (247141023) - 60876000 -> 72900001 (116680003) View
116680003 \|Is a (attribute)\|	72900001 \|Familial multiple polyposis syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
254594009 View
254594009	Hamartoma of intestine (disorder)	Hamartoma of intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
399960008 View
399960008	Congenital hamartoma (disorder)	Hamartomatosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
72900001 View
72900001	Familial multiple polyposis syndrome (disorder)	Polyposis coli	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1492007 View
1492007	Congenital anomaly of large intestine (disorder)	Congenital anomaly of large intestine	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 (27ce2537-d4b1-570b-8f26-7e5f33e9a76b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D12.6	TRUE	ALWAYS D12.6 \| POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE	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)\|
ExtendedMap object (2821ba31-9893-5774-a257-a95ddb5b4305) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	SOURCE SNOMED CONCEPT IS AMBIGUOUS	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447640006 \|Source snomed concept is ambiguous (foundation metadata concept)\|

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