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Terminology chevron_right Concepts chevron_right 81848006

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Incomplete unilateral congenital failure of fusion (morphologic abnormality)

Shortest Term

Incomplete unilateral congenital failure of fusion

Definition Status

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Incomplete unilateral congenital failure of fusion (morphologic abnormality)

SCTID: 81848006, Primitive, Inactive

81848006|Incomplete unilateral congenital failure of fusion (morphologic abnormality)|

Expression

81848006 |Incomplete unilateral congenital failure of fusion (morphologic abnormality)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
135778016 - Incomplete unilateral congenital failure of fusion (en) View
135778016	en	Synonym (core metadata concept)	Incomplete unilateral congenital failure of fusion	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
823164011 - Incomplete unilateral congenital failure of fusion (morphologic abnormality) (en) View
823164011	en	Fully specified name (core metadata concept)	Incomplete unilateral congenital failure of fusion (morphologic abnormality)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (281011029) - 81848006 -> 4541003 (116680003) View
116680003 \|Is a (attribute)\|	4541003 \|Congenital failure of fusion (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

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help

Descriptions