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Terminology chevron_right Concepts chevron_right 68926002

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Component

68926002

The component that hold information about this concept.

Fully Specified Name (FSN)

Idiopathic arterial calcification of infancy (disorder)

Shortest Term

Idiopathic arterial calcification of infancy

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 arterial calcification of infancy (disorder)

SCTID: 68926002, Defined, Active

68926002|Idiopathic arterial calcification of infancy (disorder)|

en Idiopathic arterial calcification of infancy
en Idiopathic arterial calcification of infancy (disorder)

Expression

68926002 |Idiopathic arterial calcification of infancy (disorder)|
 === 461415008 |Hereditary dysplasia of blood vessel (disorder)| + 
41969006 |Idiopathic disease (disorder)| + 
237897009 |Vascular calcification (disorder)| + 
359557001 |Disorder of artery (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 51114001 |Arterial structure (body structure)|,
246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
114481010 - Idiopathic arterial calcification of infancy (en) View
114481010	en	Synonym (core metadata concept)	Idiopathic arterial calcification of infancy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
808815012 - Idiopathic arterial calcification of infancy (disorder) (en) View
808815012	en	Fully specified name (core metadata concept)	Idiopathic arterial calcification of infancy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13665563022) - 68926002 -> 41969006 (116680003) View
116680003 \|Is a (attribute)\|	41969006 \|Idiopathic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13665596024) - 68926002 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4675781023) - 68926002 -> 461415008 (116680003) View
116680003 \|Is a (attribute)\|	461415008 \|Hereditary dysplasia of blood vessel (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (846076021) - 68926002 -> 18115005 (116676008) View
116676008 \|Associated morphology (attribute)\|	18115005 \|Pathologic calcification, calcified structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (846077028) - 68926002 -> 51114001 (363698007) View
363698007 \|Finding site (attribute)\|	51114001 \|Arterial structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3395646022) - 68926002 -> 51114001 (363698007) View
363698007 \|Finding site (attribute)\|	51114001 \|Arterial structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3395647029) - 68926002 -> 18115005 (116676008) View
116676008 \|Associated morphology (attribute)\|	18115005 \|Pathologic calcification, calcified structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2842816020) - 68926002 -> 237897009 (116680003) View
116680003 \|Is a (attribute)\|	237897009 \|Vascular calcification (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (260222023) - 68926002 -> 359557001 (116680003) View
116680003 \|Is a (attribute)\|	359557001 \|Disorder of artery (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
461415008 View
461415008	Hereditary dysplasia of blood vessel (disorder)	Hereditary dysplasia of blood vessel	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237897009 View
237897009	Vascular calcification (disorder)	Vascular calcification	900000000000073002 \|Sufficiently defined by necessary conditions 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
359557001 View
359557001	Disorder of artery (disorder)	Bệnh động mạch	900000000000073002 \|Sufficiently defined by necessary conditions 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 (bbba6aaa-af40-56bd-bb6a-1c2916c9f94a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	I70.90	TRUE	ALWAYS I70.90 \| MAPPED FOLLOWING WHO GUIDANCE	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 (eac62d09-ff05-52d9-bac3-4b527ac0378c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q28.8	TRUE	ALWAYS Q28.8	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)\|

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