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Terminology chevron_right Concepts chevron_right 126764002

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Component

126764002

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of intestinal tract (disorder)

Shortest Term

Congenital anomaly of 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 anomaly of intestinal tract (disorder)

SCTID: 126764002, Defined, Active

126764002|Congenital anomaly of intestinal tract (disorder)|

en Congenital anomaly of intestinal tract
en Congenital anomaly of intestinal tract (disorder)

Expression

126764002 |Congenital anomaly of intestinal tract (disorder)|
 === 85919009 |Disorder of intestine (disorder)| + 
128347007 |Congenital anomaly of gastrointestinal tract (disorder)| + 
128332003 |Congenital anomaly of digestive organ (disorder)| + 
363024001 |Congenital anomaly of abdomen (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (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
145318011 - Congenital anomaly of intestinal tract (en) View
145318011	en	Synonym (core metadata concept)	Congenital anomaly of intestinal tract	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
730770018 - Congenital anomaly of intestinal tract (disorder) (en) View
730770018	en	Fully specified name (core metadata concept)	Congenital anomaly of intestinal tract (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (160950026) - 126764002 -> 128347007 (116680003) View
116680003 \|Is a (attribute)\|	128347007 \|Congenital anomaly of gastrointestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2687810024) - 126764002 -> 31686000 (116680003) View
116680003 \|Is a (attribute)\|	31686000 \|Congenital anomaly of lower alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15923118026) - 126764002 -> 363024001 (116680003) View
116680003 \|Is a (attribute)\|	363024001 \|Congenital anomaly of abdomen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (692980026) - 126764002 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4971762022) - 126764002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4971763028) - 126764002 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4995754027) - 126764002 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6096619026) - 126764002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10531934022) - 126764002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10531935023) - 126764002 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2590321020) - 126764002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3427927026) - 126764002 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3427928020) - 126764002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1755902028) - 126764002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2543403020) - 126764002 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2543402026) - 126764002 -> 128332003 (116680003) View
116680003 \|Is a (attribute)\|	128332003 \|Congenital anomaly of digestive organ (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1755901024) - 126764002 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (160948023) - 126764002 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (692979029) - 126764002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (160949026) - 126764002 -> 85919009 (116680003) View
116680003 \|Is a (attribute)\|	85919009 \|Disorder of intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
128347007 View
128347007	Congenital anomaly of gastrointestinal tract (disorder)	Gastrointestinal tract congenital anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363024001 View
363024001	Congenital anomaly of abdomen (disorder)	Congenital anomaly of abdomen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85919009 View
85919009	Disorder of intestine (disorder)	Enteropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128332003 View
128332003	Congenital anomaly of digestive organ (disorder)	Congenital anomaly of digestive organ	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1222675000 View
1222675000	Primary desmosis coli (disorder)	Primary desmosis coli	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
93386004 View
93386004	Congenital stenosis of intestinal tract (disorder)	Congenital narrowed intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
253792003 View
253792003	Congenital diverticulosis (disorder)	Congenital diverticulosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
770900000 View
770900000	Familial omphalocele syndrome with facial dysmorphism (disorder)	Familial omphalocele syndrome with facial dysmorphism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
725591002 View
725591002	Congenital enterocyte heparan sulfate deficiency (disorder)	Congenital enterocyte heparan sulfate deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
719833004 View
719833004	Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome (disorder)	Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722060007 View
722060007	Oculogastrointestinal muscular dystrophy (disorder)	Oculogastrointestinal muscular dystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
3845008 View
3845008	Congenital duplication of intestine (disorder)	Duplication of intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
91890003 View
91890003	Congenital absence of intestinal tract (disorder)	Agenesis of intestinal tract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
204748003 View
204748003	Congenital intestinal adhesions (disorder)	Congenital intestinal adhesions	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
3886001 View
3886001	Congenital fecaliths (disorder)	Congenital fecaliths	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93268000 View
93268000	Congenital hypoplasia of intestinal tract (disorder)	Congenital short intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93330004 View
93330004	Congenital malposition of intestinal tract (disorder)	Congenital malpositioned intestinal tract	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
55193002 View
55193002	Congenital anomaly of small intestine (disorder)	Congenital anomaly of small intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
58037000 View
58037000	Cowden syndrome (disorder)	Cowden syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
61108006 View
61108006	Ectopic intestinal mucosa (disorder)	Ectopic intestinal mucosa	900000000000073002 \|Sufficiently defined by necessary conditions 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
93058003 View
93058003	Congenital dilatation of intestinal tract (disorder)	Congenital enteromegaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93063004 View
93063004	Congenital diverticulum of intestinal tract (disorder)	Congenital diverticula of the intestine	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93091007 View
93091007	Congenital fistula of intestinal tract (disorder)	Congenital fistula of intestinal tract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
129601002 View
129601002	Congenital neurogenic ileus syndrome (disorder)	Jirasek-zuelzer-wilson syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253783001 View
253783001	Neuronal intestinal dysplasia (disorder)	Neuronal intestinal dysplasia	900000000000074008 \|Necessary but not sufficient concept 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 (9ee56c01-1775-5a64-8bb3-b5109f0efbd6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q43.9	TRUE	ALWAYS Q43.9	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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