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Terminology chevron_right Concepts chevron_right 95501007

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Component

95501007

The component that hold information about this concept.

Fully Specified Name (FSN)

Retinal arteriovenous malformation (disorder)

Shortest Term

Retinal arteriovenous anomaly

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

Retinal arteriovenous malformation (disorder)

SCTID: 95501007, Defined, Active

95501007|Retinal arteriovenous malformation (disorder)|

en Congenital retinal arteriovenous anastomoses
en Congenital retinal arteriovenous communication
en Congenital arteriovenous malformation of retina
en Retinal arteriovenous anomaly
en Retinal arteriovenous malformation
en Retinal arteriovenous malformation (disorder)

Expression

95501007 |Retinal arteriovenous malformation (disorder)|
 === 2818004 |Congenital vascular anomaly of eye (disorder)| + 
49381001 |Congenital anomaly of retina (disorder)| + 
234141001 |Congenital arteriovenous malformation (disorder)| + 
897413005 |Structural abnormality of blood vessel of retina (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 24551003 |Arteriovenous malformation (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 28758002 |Structure of blood vessel of retina (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5066444016 - Congenital retinal arteriovenous anastomoses (en) View
5066444016	en	Synonym (core metadata concept)	Congenital retinal arteriovenous anastomoses	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
5066445015 - Congenital retinal arteriovenous communication (en) View
5066445015	en	Synonym (core metadata concept)	Congenital retinal arteriovenous communication	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3781220018 - Congenital arteriovenous malformation of retina (en) View
3781220018	en	Synonym (core metadata concept)	Congenital arteriovenous malformation of retina	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1235918014 - Retinal arteriovenous anomaly (en) View
1235918014	en	Synonym (core metadata concept)	Retinal arteriovenous anomaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
158183011 - Retinal arteriovenous malformation (en) View
158183011	en	Synonym (core metadata concept)	Retinal arteriovenous malformation	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
839669016 - Retinal arteriovenous malformation (disorder) (en) View
839669016	en	Fully specified name (core metadata concept)	Retinal arteriovenous malformation (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (307290025) - 95501007 -> 57534004 (116680003) View
116680003 \|Is a (attribute)\|	57534004 \|Retinal vascular disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16353174020) - 95501007 -> 897413005 (116680003) View
116680003 \|Is a (attribute)\|	897413005 \|Structural abnormality of blood vessel of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (307288026) - 95501007 -> 2818004 (116680003) View
116680003 \|Is a (attribute)\|	2818004 \|Congenital vascular anomaly of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4971372022) - 95501007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4977246024) - 95501007 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4977248020) - 95501007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4977249028) - 95501007 -> 24551003 (116676008) View
116676008 \|Associated morphology (attribute)\|	24551003 \|Arteriovenous malformation (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4977250028) - 95501007 -> 59820001 (363698007) View
363698007 \|Finding site (attribute)\|	59820001 \|Blood vessel structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5002695029) - 95501007 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10530574025) - 95501007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10530575029) - 95501007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (929902029) - 95501007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (929899027) - 95501007 -> 28758002 (363698007) View
363698007 \|Finding site (attribute)\|	28758002 \|Structure of blood vessel of retina (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2455784027) - 95501007 -> 24551003 (116676008) View
116676008 \|Associated morphology (attribute)\|	24551003 \|Arteriovenous malformation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3382227023) - 95501007 -> 28758002 (363698007) View
363698007 \|Finding site (attribute)\|	28758002 \|Structure of blood vessel of retina (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3458805022) - 95501007 -> 24551003 (116676008) View
116676008 \|Associated morphology (attribute)\|	24551003 \|Arteriovenous malformation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (929900021) - 95501007 -> 24551003 (116676008) View
116676008 \|Associated morphology (attribute)\|	24551003 \|Arteriovenous malformation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1785013023) - 95501007 -> 280951005 (363698007) View
363698007 \|Finding site (attribute)\|	280951005 \|Visual pathway structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2272047029) - 95501007 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2272048023) - 95501007 -> 51114001 (363698007) View
363698007 \|Finding site (attribute)\|	51114001 \|Arterial structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2272049026) - 95501007 -> 29092000 (363698007) View
363698007 \|Finding site (attribute)\|	29092000 \|Venous structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2217852028) - 95501007 -> 24551003 (116676008) View
116676008 \|Associated morphology (attribute)\|	24551003 \|Arteriovenous malformation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1688503024) - 95501007 -> 61136001 (116680003) View
116680003 \|Is a (attribute)\|	61136001 \|Congenital vascular disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2233866026) - 95501007 -> 234141001 (116680003) View
116680003 \|Is a (attribute)\|	234141001 \|Congenital arteriovenous malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (929901020) - 95501007 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (307289023) - 95501007 -> 49381001 (116680003) View
116680003 \|Is a (attribute)\|	49381001 \|Congenital anomaly of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
897413005 View
897413005	Structural abnormality of blood vessel of retina (disorder)	Abnormal retinal vascular morphology	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
234141001 View
234141001	Congenital arteriovenous malformation (disorder)	Arteriovenous malformation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
2818004 View
2818004	Congenital vascular anomaly of eye (disorder)	Congenital vascular anomaly of eye	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
49381001 View
49381001	Congenital anomaly of retina (disorder)	Congenital anomaly of retina	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
247127002 View
247127002	Retinal arteriovenous shunt (disorder)	Retinal arteriovenous shunt	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 (0c19abc7-386e-50eb-aa13-0b6a85bbd158) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q14.1	TRUE	ALWAYS Q14.1	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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