dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 16301006

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital opacity (morphologic abnormality)

Shortest Term

Congenital opacity

Definition Status

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

Summary

Congenital opacity (morphologic abnormality)

SCTID: 16301006, Primitive, Inactive

16301006|Congenital opacity (morphologic abnormality)|

Expression

16301006 |Congenital opacity (morphologic abnormality)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
27594019 - Congenital opacity (en) View
27594019	en	Synonym (core metadata concept)	Congenital opacity	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
743300015 - Congenital opacity (morphologic abnormality) (en) View
743300015	en	Fully specified name (core metadata concept)	Congenital opacity (morphologic abnormality)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
27595018 - Congenital opacity, NOS (en) View
27595018	en	Synonym (core metadata concept)	Congenital opacity, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
27596017 - Congenital thickening, NOS (en) View
27596017	en	Synonym (core metadata concept)	Congenital thickening, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5004591028) - 16301006 -> 21390004 (116680003) View
116680003 \|Is a (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (172617021) - 16301006 -> 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

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

Descriptions