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Terminology chevron_right Concepts chevron_right 201673008

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial chondrocalcinosis (disorder)

Shortest Term

Familial chondrocalcinosis

Definition Status

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

Summary

Familial chondrocalcinosis (disorder)

SCTID: 201673008, Primitive, Inactive

201673008|Familial chondrocalcinosis (disorder)|

Expression

201673008 |Familial chondrocalcinosis (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
309684018 - Familial chondrocalcinosis (en) View
309684018	en	Synonym (core metadata concept)	Familial chondrocalcinosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2728494015 - Familial chondrocalcinosis (disorder) (en) View
2728494015	en	Fully specified name (core metadata concept)	Familial chondrocalcinosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
586570014 - Familial chondrocalcinosis (en) View
586570014	en	Fully specified name (core metadata concept)	Familial chondrocalcinosis	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