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Terminology chevron_right Concepts chevron_right 720512007

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Component

720512007

The component that hold information about this concept.

Fully Specified Name (FSN)

Arterial dissection and lentiginosis syndrome (disorder)

Shortest Term

Arterial dissection and lentiginosis syndrome

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

Arterial dissection and lentiginosis syndrome (disorder)

SCTID: 720512007, Primitive, Active

720512007|Arterial dissection and lentiginosis syndrome (disorder)|

en Arterial dissection and lentiginosis syndrome
en Arterial dissection and lentiginosis syndrome (disorder)

Expression

720512007 |Arterial dissection and lentiginosis syndrome (disorder)|
 <<< 363005004 |Cardiovascular system hereditary disorder (disorder)| + 
710864009 |Dissection of artery (disorder)| + 
234119001 |Arterial malformation (disorder)| + 
86042009 |Congenital melanosis (disorder)| + 
400083002 |Congenital hamartoma of skin (disorder)| + 
402624000 |Lentiginosis (disorder)| + 
403804008 |Hereditary hypermelanosis (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 767376003 |Lentigo (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 5399005 |Dissecting hemorrhage (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 710863003 |Structure of wall of artery (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
3321086017 - Arterial dissection and lentiginosis syndrome (en) View
3321086017	en	Synonym (core metadata concept)	Arterial dissection and lentiginosis syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3321085018 - Arterial dissection and lentiginosis syndrome (disorder) (en) View
3321085018	en	Fully specified name (core metadata concept)	Arterial dissection and lentiginosis syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10518263028) - 720512007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12091175029) - 720512007 -> 205564003 (116680003) View
116680003 \|Is a (attribute)\|	205564003 \|Congenital pigmentary skin anomalies (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069230028) - 720512007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358227026) - 720512007 -> 765195000 (116680003) View
116680003 \|Is a (attribute)\|	765195000 \|Familial generalized lentiginosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12091171022) - 720512007 -> 86042009 (116680003) View
116680003 \|Is a (attribute)\|	86042009 \|Congenital melanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12091172026) - 720512007 -> 400083002 (116680003) View
116680003 \|Is a (attribute)\|	400083002 \|Congenital hamartoma of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12091174025) - 720512007 -> 402624000 (116680003) View
116680003 \|Is a (attribute)\|	402624000 \|Lentiginosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12209805026) - 720512007 -> 403804008 (116680003) View
116680003 \|Is a (attribute)\|	403804008 \|Hereditary hypermelanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6687362021) - 720512007 -> 5399005 (116676008) View
116676008 \|Associated morphology (attribute)\|	5399005 \|Dissecting hemorrhage (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6687363027) - 720512007 -> 710863003 (363698007) View
363698007 \|Finding site (attribute)\|	710863003 \|Structure of wall of artery (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9358224022) - 720512007 -> 767376003 (116676008) View
116676008 \|Associated morphology (attribute)\|	767376003 \|Lentigo (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9358225023) - 720512007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10518262022) - 720512007 -> 234119001 (116680003) View
116680003 \|Is a (attribute)\|	234119001 \|Arterial malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518264023) - 720512007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518265024) - 720512007 -> 5399005 (116676008) View
116676008 \|Associated morphology (attribute)\|	5399005 \|Dissecting hemorrhage (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518266020) - 720512007 -> 767376003 (116676008) View
116676008 \|Associated morphology (attribute)\|	767376003 \|Lentigo (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518267027) - 720512007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518268021) - 720512007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518269029) - 720512007 -> 710863003 (363698007) View
363698007 \|Finding site (attribute)\|	710863003 \|Structure of wall of artery (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6578297029) - 720512007 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6687360029) - 720512007 -> 402777004 (116680003) View
116680003 \|Is a (attribute)\|	402777004 \|Hereditary lentiginosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6687365023) - 720512007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6687367026) - 720512007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6690025025) - 720512007 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6920331029) - 720512007 -> 724839001 (116680003) View
116680003 \|Is a (attribute)\|	724839001 \|Genetic disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9358226024) - 720512007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6687359023) - 720512007 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6687358026) - 720512007 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6687361025) - 720512007 -> 710864009 (116680003) View
116680003 \|Is a (attribute)\|	710864009 \|Dissection of artery (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
403804008 View
403804008	Hereditary hypermelanosis (disorder)	Hereditary hypermelanosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
86042009 View
86042009	Congenital melanosis (disorder)	Congenital melanosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
402624000 View
402624000	Lentiginosis (disorder)	Tàn nhang	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
710864009 View
710864009	Dissection of artery (disorder)	Arterial dissection	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
400083002 View
400083002	Congenital hamartoma of skin (disorder)	Congenital hamartoma of skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
234119001 View
234119001	Arterial malformation (disorder)	Arterial malformation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363005004 View
363005004	Cardiovascular system hereditary disorder (disorder)	Cardiovascular system hereditary disorder	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 (103401e2-e728-50fb-9b54-831df5caadb2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	TRUE	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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