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Terminology chevron_right Concepts chevron_right 253778009

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Component

253778009

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital functional disorders of the colon (disorder)

Shortest Term

Congenital functional disorders of the colon

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

Congenital functional disorders of the colon (disorder)

SCTID: 253778009, Primitive, Active

253778009|Congenital functional disorders of the colon (disorder)|

en Congenital functional disorders of the colon
en Congenital functional disorders of the colon (disorder)

Expression

253778009 |Congenital functional disorders of the colon (disorder)|
 <<< 128524007 |Disorder of colon (disorder)| + 
66091009 |Congenital disease (disorder)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)|
        { 363698007 |Finding site (attribute)| = 71854001 |Colon 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
377860014 - Congenital functional disorders of the colon (en) View
377860014	en	Synonym (core metadata concept)	Congenital functional disorders of the colon	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
644578018 - Congenital functional disorders of the colon (disorder) (en) View
644578018	en	Fully specified name (core metadata concept)	Congenital functional disorders of the colon (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15880857026) - 253778009 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (73833025) - 253778009 -> 1492007 (116680003) View
116680003 \|Is a (attribute)\|	1492007 \|Congenital anomaly of large intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2579007027) - 253778009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3348252027) - 253778009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3462263029) - 253778009 -> 71854001 (363698007) View
363698007 \|Finding site (attribute)\|	71854001 \|Colon structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4984846026) - 253778009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5043527025) - 253778009 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5043528024) - 253778009 -> 71854001 (363698007) View
363698007 \|Finding site (attribute)\|	71854001 \|Colon structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (577958028) - 253778009 -> 71854001 (363698007) View
363698007 \|Finding site (attribute)\|	71854001 \|Colon structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1736055021) - 253778009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (73832024) - 253778009 -> 31686000 (116680003) View
116680003 \|Is a (attribute)\|	31686000 \|Congenital anomaly of lower alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1736056022) - 253778009 -> 14742008 (363698007) View
363698007 \|Finding site (attribute)\|	14742008 \|Large intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (577959020) - 253778009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (73831028) - 253778009 -> 128524007 (116680003) View
116680003 \|Is a (attribute)\|	128524007 \|Disorder of colon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128524007 View
128524007	Disorder of colon (disorder)	Disease of colon	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
253782006 View
253782006	Small left colon syndrome (disorder)	Small left colon syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
18389004 View
18389004	Microcolon (disorder)	Microcolon	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253781004 View
253781004	Megacystis, microcolon, hypoperistalsis syndrome (disorder)	Berdon syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253784007 View
253784007	Hyperganglionosis (disorder)	Hyperganglionosis	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 (685187df-1dad-5e7a-8df1-48bf43c54f07) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q43.2	TRUE	ALWAYS Q43.2	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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