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Terminology chevron_right Concepts chevron_right 19577007

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Hypocupremia (disorder)

Shortest Term

Hypocupremia

Definition Status

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

Summary

Hypocupremia (disorder)

SCTID: 19577007, Primitive, Active

19577007|Hypocupremia (disorder)|

Expression

19577007 |Hypocupremia (disorder)|
 <<< 111379007 |Mineral deficiency (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
32962018 - Chronic copper deficiency (en) View
32962018	en	Synonym (core metadata concept)	Chronic copper deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
479672013 - Copper deficiency (en) View
479672013	en	Synonym (core metadata concept)	Copper deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
479673015 - Hypocupraemia (en) View
479673015	en	Synonym (core metadata concept)	Hypocupraemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
32960014 - Hypocupremia (en) View
32960014	en	Synonym (core metadata concept)	Hypocupremia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
747850015 - Hypocupremia (disorder) (en) View
747850015	en	Fully specified name (core metadata concept)	Hypocupremia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
32961013 - Hypocupremia, NOS (en) View
32961013	en	Synonym (core metadata concept)	Hypocupremia, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (179128020) - 19577007 -> 238120004 (116680003) View
116680003 \|Is a (attribute)\|	238120004 \|Trace element deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12064603028) - 19577007 -> 111379007 (116680003) View
116680003 \|Is a (attribute)\|	111379007 \|Mineral deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (720323024) - 19577007 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (179127026) - 19577007 -> 79886009 (116680003) View
116680003 \|Is a (attribute)\|	79886009 \|Disorder of copper metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
111379007 View
111379007	Mineral deficiency (disorder)	Mineral deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
763531001 View
763531001	Familial benign copper deficiency (disorder)	Familial benign hypocupremia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (c7ec5e5d-400e-55b2-976e-c735a437b218) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E61.0	TRUE	ALWAYS E61.0 \| 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