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Terminology chevron_right Concepts chevron_right 736703007

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Carrier of hemochromatosis hfe gene mutation (finding)

Shortest Term

Carrier of hemochromatosis hfe gene mutation

Definition Status

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

Summary

Carrier of hemochromatosis hfe gene mutation (finding)

SCTID: 736703007, Primitive, Active

736703007|Carrier of hemochromatosis hfe gene mutation (finding)|

Expression

736703007 |Carrier of hemochromatosis hfe gene mutation (finding)|
 <<< 29679002 |Carrier of disorder (finding)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2006400 - Người mang đột biến gen HFE gây bệnh ứ sắt (phát hiện) (vi) View
2006400	vi	Synonym (core metadata concept)	Người mang đột biến gen HFE gây bệnh ứ sắt (phát hiện)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3521971016 - Carrier of haemochromatosis HFE gene mutation (en) View
3521971016	en	Synonym (core metadata concept)	Carrier of haemochromatosis HFE gene mutation	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3521973018 - Carrier of hemochromatosis HFE gene mutation (en) View
3521973018	en	Synonym (core metadata concept)	Carrier of hemochromatosis HFE gene mutation	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3521972011 - Carrier of hemochromatosis HFE gene mutation (finding) (en) View
3521972011	en	Fully specified name (core metadata concept)	Carrier of hemochromatosis HFE gene mutation (finding)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7237707021) - 736703007 -> 278844005 (363714003) View
363714003 \|Interprets (attribute)\|	278844005 \|General clinical state (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7237706028) - 736703007 -> 29679002 (116680003) View
116680003 \|Is a (attribute)\|	29679002 \|Carrier of disorder (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
29679002 View
29679002	Carrier of disorder (finding)	Carrier	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

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
ExtendedMap object (3457d460-adbd-57b7-bbbf-49351c62f94b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

Descriptions