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Terminology chevron_right Concepts chevron_right 93032003

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Component

93032003

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital atresia of intestinal tract (disorder)

Shortest Term

Imperforate intestinal tract

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 atresia of intestinal tract (disorder)

SCTID: 93032003, Defined, Active

93032003|Congenital atresia of intestinal tract (disorder)|

en Congenital atresia of intestinal tract
en Congenital atresia of intestinal tract (disorder)
en Imperforate intestinal tract

Expression

93032003 |Congenital atresia of intestinal tract (disorder)|
 === 126764002 |Congenital anomaly of intestinal tract (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
153881013 - Congenital atresia of intestinal tract (en) View
153881013	en	Synonym (core metadata concept)	Congenital atresia of intestinal tract	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
836681018 - Congenital atresia of intestinal tract (disorder) (en) View
836681018	en	Fully specified name (core metadata concept)	Congenital atresia of intestinal tract (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
153882018 - Imperforate intestinal tract (en) View
153882018	en	Synonym (core metadata concept)	Imperforate intestinal tract	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (913599029) - 93032003 -> 56457002 (116676008) View
116676008 \|Associated morphology (attribute)\|	56457002 \|Congenital atresia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15893223028) - 93032003 -> 1303493008 (116676008) View
116676008 \|Associated morphology (attribute)\|	1303493008 \|Atresia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3379723028) - 93032003 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4972364023) - 93032003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4996094026) - 93032003 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5008106027) - 93032003 -> 56457002 (116676008) View
116676008 \|Associated morphology (attribute)\|	56457002 \|Congenital atresia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6092802028) - 93032003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532336025) - 93032003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2552841020) - 93032003 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2604283029) - 93032003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3379722022) - 93032003 -> 56457002 (116676008) View
116676008 \|Associated morphology (attribute)\|	56457002 \|Congenital atresia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2448754029) - 93032003 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (301439021) - 93032003 -> 31686000 (116680003) View
116680003 \|Is a (attribute)\|	31686000 \|Congenital anomaly of lower alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (913601027) - 93032003 -> 5668004 (363698007) View
363698007 \|Finding site (attribute)\|	5668004 \|Lower gastrointestinal tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2049089029) - 93032003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2698829029) - 93032003 -> 126764002 (116680003) View
116680003 \|Is a (attribute)\|	126764002 \|Congenital anomaly of intestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (913598021) - 93032003 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2217063029) - 93032003 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2198125028) - 93032003 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1686203025) - 93032003 -> 95470009 (116680003) View
116680003 \|Is a (attribute)\|	95470009 \|Congenital anomaly of digestive tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (913600026) - 93032003 -> 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
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

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1363062007 View
1363062007	Isolated multiple intestinal atresia (disorder)	Isolated multiple intestinal atresia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1197428008 View
1197428008	Combined immunodeficiency, enteropathy spectrum (disorder)	Combined immunodeficiency due to ttc7a mutation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1003397007 View
1003397007	Congenital atresia of intestine at multiple levels (disorder)	Multiple-level intestinal atresia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773673002 View
773673002	Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome (disorder)	Hội chứng giảm sản tuyến tụy, tịt ruột, giảm sản túi mật	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
735719008 View
735719008	Neonatal intestinal perforation co-occurrent and due to intestinal atresia (disorder)	Neonatal intestinal perforation with intestinal atresia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
762273001 View
762273001	Fetal intrauterine intestinal perforation co-occurrent and due to congenital atresia of intestinal tract (disorder)	Fetal intrauterine intestinal perforation with congenital atresia of intestinal tract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
719844007 View
719844007	Ulceration of umbilical cord and atresia of intestine syndrome (disorder)	Umbilical cord ulceration with intestinal atresia syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
84296002 View
84296002	Congenital atresia of small intestine (disorder)	Apple-peel syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
204711007 View
204711007	Atresia of large intestine (disorder)	Atresia of large intestine	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 (d42c5c1b-7844-5428-90f3-a8ccb83b4626) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q41.9	TRUE	ALWAYS Q41.9	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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