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Terminology chevron_right Concepts chevron_right 399982001

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Component

399982001

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital vascular disorder (disorder)

Shortest Term

Congenital vascular disorder

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

Congenital vascular disorder (disorder)

SCTID: 399982001, Defined, Active

399982001|Congenital vascular disorder (disorder)|

en Congenital vascular abnormality
en Congenital vascular disorder
en Congenital vascular disorder (disorder)

Expression

399982001 |Congenital vascular disorder (disorder)|
 === 27550009 |Disorder of blood vessel (disorder)| + 
762228008 |Congenital cardiovascular disorder (disorder)|
        { 363698007 |Finding site (attribute)| = 59820001 |Blood vessel structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1787057013 - Congenital vascular abnormality (en) View
1787057013	en	Synonym (core metadata concept)	Congenital vascular abnormality	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1779259018 - Congenital vascular disorder (en) View
1779259018	en	Synonym (core metadata concept)	Congenital vascular disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1767902015 - Congenital vascular disorder (disorder) (en) View
1767902015	en	Fully specified name (core metadata concept)	Congenital vascular disorder (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4988856024) - 399982001 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7681191024) - 399982001 -> 762228008 (116680003) View
116680003 \|Is a (attribute)\|	762228008 \|Congenital cardiovascular disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2245715029) - 399982001 -> 9904008 (116680003) View
116680003 \|Is a (attribute)\|	9904008 \|Congenital anomaly of cardiovascular system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2284190024) - 399982001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3285446029) - 399982001 -> 239953001 (116680003) View
116680003 \|Is a (attribute)\|	239953001 \|Lesion of soft tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3533709021) - 399982001 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3550986029) - 399982001 -> 59820001 (363698007) View
363698007 \|Finding site (attribute)\|	59820001 \|Blood vessel structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4972166029) - 399982001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4988857026) - 399982001 -> 59820001 (363698007) View
363698007 \|Finding site (attribute)\|	59820001 \|Blood vessel structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2284188023) - 399982001 -> 59820001 (363698007) View
363698007 \|Finding site (attribute)\|	59820001 \|Blood vessel structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2284189026) - 399982001 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2284186022) - 399982001 -> 113257007 (363698007) View
363698007 \|Finding site (attribute)\|	113257007 \|Structure of cardiovascular system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2284187029) - 399982001 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2245716028) - 399982001 -> 27550009 (116680003) View
116680003 \|Is a (attribute)\|	27550009 \|Disorder of blood vessel (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
762228008 View
762228008	Congenital cardiovascular disorder (disorder)	Congenital cardiovascular disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
27550009 View
27550009	Disorder of blood vessel (disorder)	Angiopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
254778000 View
254778000	Congenital livedo reticularis (disorder)	Van lohuizen syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
771515001 View
771515001	Facial dysmorphism, immunodeficiency, livedo, short stature syndrome (disorder)	Fils syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
42866003 View
42866003	Congenital coronary artery sclerosis (disorder)	Congenital coronary artery sclerosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
32361000119104 View
32361000119104	Congenital hemangioma (disorder)	Congenital hemangioma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
234153002 View
234153002	Congenital arteriovenous fistula infection (disorder)	Congenital arteriovenous fistula infection	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
400159008 View
400159008	Congenital vascular malformation (disorder)	Vascular malformation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
36025004 View
36025004	Fibrous skin tumor of tuberous sclerosis (disorder)	Pringle tumor	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
236759008 View
236759008	Congenital familial idiopathic priapism (disorder)	Congenital familial idiopathic priapism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253340009 View
253340009	Prominent valve of inferior vena cava (disorder)	Prominent eustachian valve	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
254775002 View
254775002	Bregeat's syndrome (disorder)	Bregeat 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 (c4e2f24d-fffc-5196-9f5f-f80858f0766b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q27.9	TRUE	ALWAYS Q27.9	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 399982001

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