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Terminology chevron_right Concepts chevron_right 60115006

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Component

60115006

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital malposition (morphologic abnormality)

Shortest Term

Situs perversus

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 malposition (morphologic abnormality)

SCTID: 60115006, Primitive, Inactive

60115006|Congenital malposition (morphologic abnormality)|

en Congenital abnormal position
en Congenital malposition
en Congenital malposition (morphologic abnormality)
en Situs perversus

Expression

60115006 |Congenital malposition (morphologic abnormality)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
99869012 - Congenital abnormal position (en) View
99869012	en	Synonym (core metadata concept)	Congenital abnormal position	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
99865018 - Congenital malposition (en) View
99865018	en	Synonym (core metadata concept)	Congenital malposition	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
799032017 - Congenital malposition (morphologic abnormality) (en) View
799032017	en	Fully specified name (core metadata concept)	Congenital malposition (morphologic abnormality)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
99868016 - Situs perversus (en) View
99868016	en	Synonym (core metadata concept)	Situs perversus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
99867014 - Congenital abnormal position, NOS (en) View
99867014	en	Synonym (core metadata concept)	Congenital abnormal position, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
99870013 - Congenital dislocation, NOS (en) View
99870013	en	Synonym (core metadata concept)	Congenital dislocation, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
99866017 - Congenital malposition, NOS (en) View
99866017	en	Synonym (core metadata concept)	Congenital malposition, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
99871012 - Developmental dislocation, NOS (en) View
99871012	en	Synonym (core metadata concept)	Developmental dislocation, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2549075026) - 60115006 -> 408737001 (116680003) View
116680003 \|Is a (attribute)\|	408737001 \|Malposition (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4999959023) - 60115006 -> 21390004 (116680003) View
116680003 \|Is a (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (245892025) - 60115006 -> 107656002 (116680003) View
116680003 \|Is a (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (245893024) - 60115006 -> 52028006 (116680003) View
116680003 \|Is a (attribute)\|	52028006 \|Malposition (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

Terminology chevron_right Concepts chevron_right 60115006

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