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Terminology chevron_right Concepts chevron_right 547009

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Component

547009

The component that hold information about this concept.

Fully Specified Name (FSN)

Hypersecretion of calcitonin (disorder)

Shortest Term

Hypersecretion of calcitonin

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

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

Summary

Hypersecretion of calcitonin (disorder)

SCTID: 547009, Primitive, Active

547009|Hypersecretion of calcitonin (disorder)|

en Hypersecretion of calcitonin
en Hypersecretion of calcitonin (disorder)
en Hypersecretion of thyrocalcitonin

Expression

547009 |Hypersecretion of calcitonin (disorder)|
 <<< 14304000 |Disorder of thyroid gland (disorder)| : 
        { 363698007 |Finding site (attribute)| = 69748006 |Thyroid structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1985012 - Hypersecretion of calcitonin (en) View
1985012	en	Synonym (core metadata concept)	Hypersecretion of calcitonin	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
792961017 - Hypersecretion of calcitonin (disorder) (en) View
792961017	en	Fully specified name (core metadata concept)	Hypersecretion of calcitonin (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1986013 - Hypersecretion of thyrocalcitonin (en) View
1986013	en	Synonym (core metadata concept)	Hypersecretion of thyrocalcitonin	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (809663026) - 547009 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (809662020) - 547009 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (237068022) - 547009 -> 14304000 (116680003) View
116680003 \|Is a (attribute)\|	14304000 \|Disorder of thyroid gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
14304000 View
14304000	Disorder of thyroid gland (disorder)	Bệnh tuyến giáp	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
237552009 View
237552009	C-cell hyperplasia of thyroid (disorder)	C-cell hyperplasia of thyroid	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 (863dd839-a76e-53c6-9d9e-251b458e87b1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E07.0	TRUE	ALWAYS E07.0	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)\|

Terminology chevron_right Concepts chevron_right 547009

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