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Terminology chevron_right Concepts chevron_right 204697003

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Component

204697003

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital absence of ileum (disorder)

Shortest Term

Congenital absence of ileum

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 absence of ileum (disorder)

SCTID: 204697003, Defined, Active

204697003|Congenital absence of ileum (disorder)|

en Congenital absence of ileum
en Congenital absence of ileum (disorder)

Expression

204697003 |Congenital absence of ileum (disorder)|
 === 312895004 |Disorder of ileum (disorder)| + 
29110005 |Congenital absence of small intestine (disorder)| + 
31686000 |Congenital anomaly of lower alimentary tract (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 34516001 |Ileal 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
313883010 - Congenital absence of ileum (en) View
313883010	en	Synonym (core metadata concept)	Congenital absence of ileum	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
589959011 - Congenital absence of ileum (disorder) (en) View
589959011	en	Fully specified name (core metadata concept)	Congenital absence of ileum (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15926369026) - 204697003 -> 31686000 (116680003) View
116680003 \|Is a (attribute)\|	31686000 \|Congenital anomaly of lower alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (23378022) - 204697003 -> 29110005 (116680003) View
116680003 \|Is a (attribute)\|	29110005 \|Congenital absence of small intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11165573026) - 204697003 -> 83028006 (116680003) View
116680003 \|Is a (attribute)\|	83028006 \|Congenital partial absence of alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11165574021) - 204697003 -> 55193002 (116680003) View
116680003 \|Is a (attribute)\|	55193002 \|Congenital anomaly of small intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (468866028) - 204697003 -> 34516001 (363698007) View
363698007 \|Finding site (attribute)\|	34516001 \|Ileal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4972598026) - 204697003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000448029) - 204697003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000449021) - 204697003 -> 34516001 (363698007) View
363698007 \|Finding site (attribute)\|	34516001 \|Ileal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6109444026) - 204697003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10530162020) - 204697003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11165575022) - 204697003 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2569097021) - 204697003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3349290027) - 204697003 -> 34516001 (363698007) View
363698007 \|Finding site (attribute)\|	34516001 \|Ileal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3349291028) - 204697003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (468864025) - 204697003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2531104025) - 204697003 -> 312895004 (116680003) View
116680003 \|Is a (attribute)\|	312895004 \|Disorder of ileum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (468865029) - 204697003 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (468867021) - 204697003 -> 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
31686000 View
31686000	Congenital anomaly of lower alimentary tract (disorder)	Congenital abnormality of intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
312895004 View
312895004	Disorder of ileum (disorder)	Disorder of ileum	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
29110005 View
29110005	Congenital absence of small intestine (disorder)	Congenital absence of small 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 (fd7f3919-dc1e-5e14-a5fe-b68bf5cf9047) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q41.2	TRUE	ALWAYS Q41.2	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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