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Terminology chevron_right Concepts chevron_right 1363062007

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Component

1363062007

The component that hold information about this concept.

Fully Specified Name (FSN)

Isolated multiple intestinal atresia (disorder)

Shortest Term

Isolated multiple intestinal atresia

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

Isolated multiple intestinal atresia (disorder)

SCTID: 1363062007, Primitive, Active

1363062007|Isolated multiple intestinal atresia (disorder)|

en Isolated multiple intestinal atresia
en Isolated multiple intestinal atresia (disorder)

Expression

1363062007 |Isolated multiple intestinal atresia (disorder)|
 <<< 85995004 |Autosomal recessive hereditary disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
93032003 |Congenital atresia of intestinal tract (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1303493008 |Atresia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 113276009 |Intestinal 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
5447073012 - Isolated multiple intestinal atresia (en) View
5447073012	en	Synonym (core metadata concept)	Isolated multiple intestinal atresia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5447074018 - Isolated multiple intestinal atresia (disorder) (en) View
5447074018	en	Fully specified name (core metadata concept)	Isolated multiple intestinal atresia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16324630029) - 1363062007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16324631025) - 1363062007 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16324632021) - 1363062007 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16324633027) - 1363062007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16324635023) - 1363062007 -> 1303493008 (116676008) View
116676008 \|Associated morphology (attribute)\|	1303493008 \|Atresia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16324636024) - 1363062007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16324864028) - 1363062007 -> 93032003 (116680003) View
116680003 \|Is a (attribute)\|	93032003 \|Congenital atresia of intestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16324865027) - 1363062007 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	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
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
93032003 View
93032003	Congenital atresia of intestinal tract (disorder)	Imperforate intestinal tract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	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 (07efd5c7-ed1b-5869-a2da-991748a3884b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q41.9	TRUE	ALWAYS Q41.9 \| MAPPED FOLLOWING WHO GUIDANCE \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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