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Terminology chevron_right Concepts chevron_right 237654002

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Component

237654002

The component that hold information about this concept.

Fully Specified Name (FSN)

Idiopathic hypoparathyroidism (disorder)

Shortest Term

Idiopathic hypoparathyroidism

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Idiopathic hypoparathyroidism (disorder)

SCTID: 237654002, Defined, Active

237654002|Idiopathic hypoparathyroidism (disorder)|

en Idiopathic hypoparathyroidism
en Idiopathic hypoparathyroidism (disorder)

Expression

237654002 |Idiopathic hypoparathyroidism (disorder)|
 === 36976004 |Hypoparathyroidism (disorder)| + 
41969006 |Idiopathic disease (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 1250004 |Decreased (qualifier value)|,
363714003 |Interprets (attribute)| = 60877009 |Hormone secretion, function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 111002 |Parathyroid structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
356185013 - Idiopathic hypoparathyroidism (en) View
356185013	en	Synonym (core metadata concept)	Idiopathic hypoparathyroidism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626414018 - Idiopathic hypoparathyroidism (disorder) (en) View
626414018	en	Fully specified name (core metadata concept)	Idiopathic hypoparathyroidism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13715430026) - 237654002 -> 41969006 (116680003) View
116680003 \|Is a (attribute)\|	41969006 \|Idiopathic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526310023) - 237654002 -> 111002 (363698007) View
363698007 \|Finding site (attribute)\|	111002 \|Parathyroid structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1949736027) - 237654002 -> 42497006 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	42497006 \|Decreased hormone secretion (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9299970024) - 237654002 -> 60877009 (363714003) View
363714003 \|Interprets (attribute)\|	60877009 \|Hormone secretion, function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299971023) - 237654002 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526308021) - 237654002 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526309029) - 237654002 -> 47563007 (363714003) View
363714003 \|Interprets (attribute)\|	47563007 \|Nutritional deficiency (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53219024) - 237654002 -> 36976004 (116680003) View
116680003 \|Is a (attribute)\|	36976004 \|Hypoparathyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
36976004 View
36976004	Hypoparathyroidism (disorder)	Deficiency of pth	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
41969006 View
41969006	Idiopathic disease (disorder)	Idiopathic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
82837002 View
82837002	Kenny syndrome (disorder)	Kenny syndrome	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 (30d0903a-5144-50d1-a280-f28b98cd2a6f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E20.0	TRUE	ALWAYS E20.0	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)\|
ExtendedMap object (b0475aaf-5f97-525e-b2d5-13c091b27027) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E20.0	OTHERWISE TRUE	ALWAYS E20.0	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)\|
ExtendedMap object (e6006bef-08a4-5c29-91e4-df2e5953a8a8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	IFA 82837002 \| Kenny syndrome (disorder) \|	IF KENNY SYNDROME CHOOSE Q87.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

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