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Terminology chevron_right Concepts chevron_right 270522006

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital splenomegaly (disorder)

Shortest Term

Congenital splenomegaly

Definition Status

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

Summary

Congenital splenomegaly (disorder)

SCTID: 270522006, Primitive, Inactive

270522006|Congenital splenomegaly (disorder)|

Expression

270522006 |Congenital splenomegaly (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
405161018 - Congenital splenomegaly (en) View
405161018	en	Synonym (core metadata concept)	Congenital splenomegaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2718106019 - Congenital splenomegaly (disorder) (en) View
2718106019	en	Fully specified name (core metadata concept)	Congenital splenomegaly (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
663159014 - Congenital splenomegaly (en) View
663159014	en	Fully specified name (core metadata concept)	Congenital splenomegaly	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active

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