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Terminology chevron_right Concepts chevron_right 6426003

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Autosomal dominant analbuminemia (disorder)

Shortest Term

Autosomal dominant analbuminemia

Definition Status

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

Summary

Autosomal dominant analbuminemia (disorder)

SCTID: 6426003, Primitive, Inactive

6426003|Autosomal dominant analbuminemia (disorder)|

Expression

6426003 |Autosomal dominant analbuminemia (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
499796016 - Autosomal dominant analbuminaemia (en) View
499796016	en	Synonym (core metadata concept)	Autosomal dominant analbuminaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
11660017 - Autosomal dominant analbuminemia (en) View
11660017	en	Synonym (core metadata concept)	Autosomal dominant analbuminemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
803634012 - Autosomal dominant analbuminemia (disorder) (en) View
803634012	en	Fully specified name (core metadata concept)	Autosomal dominant analbuminemia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (252660028) - 6426003 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1774020028) - 6426003 -> 129232009 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	129232009 \|Analbuminemia (finding)\|	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
ExtendedMap object (eaebe228-df13-5865-910f-8d8354b12829) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E88.0	TRUE	ALWAYS E88.0 \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

Descriptions