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Terminology chevron_right Concepts chevron_right 8352002

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Component

8352002

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital incomplete closure (morphologic abnormality)

Shortest Term

Congenital septal defect

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 incomplete closure (morphologic abnormality)

SCTID: 8352002, Primitive, Inactive

8352002|Congenital incomplete closure (morphologic abnormality)|

en Congenital imperfect closure
en Congenital incomplete closure
en Congenital incomplete closure (morphologic abnormality)
en Congenital septal defect
en Patent embryonic structure

Expression

8352002 |Congenital incomplete closure (morphologic abnormality)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
14785015 - Congenital imperfect closure (en) View
14785015	en	Synonym (core metadata concept)	Congenital imperfect closure	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
14782017 - Congenital incomplete closure (en) View
14782017	en	Synonym (core metadata concept)	Congenital incomplete closure	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
825172010 - Congenital incomplete closure (morphologic abnormality) (en) View
825172010	en	Fully specified name (core metadata concept)	Congenital incomplete closure (morphologic abnormality)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
14788018 - Congenital septal defect (en) View
14788018	en	Synonym (core metadata concept)	Congenital septal defect	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
14787011 - Patent embryonic structure (en) View
14787011	en	Synonym (core metadata concept)	Patent embryonic structure	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
14783010 - Congenital incomplete closure, NOS (en) View
14783010	en	Synonym (core metadata concept)	Congenital incomplete closure, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
14786019 - Congenital septal defect, NOS (en) View
14786019	en	Synonym (core metadata concept)	Congenital septal defect, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
14784016 - Patent embryonic structure, NOS (en) View
14784016	en	Synonym (core metadata concept)	Patent embryonic structure, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2045073024) - 8352002 -> 4541003 (116680003) View
116680003 \|Is a (attribute)\|	4541003 \|Congenital failure of fusion (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (283910021) - 8352002 -> 107656002 (116680003) View
116680003 \|Is a (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

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