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Terminology chevron_right Concepts chevron_right 307091009

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Component

307091009

The component that hold information about this concept.

Fully Specified Name (FSN)

Factor v leiden mutation (disorder)

Shortest Term

Đột biến yếu tố v leiden

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

Factor v leiden mutation (disorder)

SCTID: 307091009, Primitive, Active

307091009|Factor v leiden mutation (disorder)|

vi Đột biến yếu tố v leiden
en Factor 5 leiden mutation
en Factor v leiden mutation
en Factor v leiden mutation (disorder)

Expression

307091009 |Factor v leiden mutation (disorder)|
 <<< 439698008 |Hereditary thrombophilia (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
591071000003116 - đột biến yếu tố V Leiden (vi) View
591071000003116	vi	Synonym (core metadata concept)	đột biến yếu tố V Leiden	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3037563018 - Factor 5 Leiden mutation (en) View
3037563018	en	Synonym (core metadata concept)	Factor 5 Leiden mutation	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
450270016 - Factor V Leiden mutation (en) View
450270016	en	Synonym (core metadata concept)	Factor V Leiden mutation	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
703570019 - Factor V Leiden mutation (disorder) (en) View
703570019	en	Fully specified name (core metadata concept)	Factor V Leiden mutation (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11288991022) - 307091009 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11288992026) - 307091009 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (134223028) - 307091009 -> 234467004 (116680003) View
116680003 \|Is a (attribute)\|	234467004 \|Thrombophilia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2722624021) - 307091009 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2783833023) - 307091009 -> 128153000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	128153000 \|Hemostatic system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3511768029) - 307091009 -> 439698008 (116680003) View
116680003 \|Is a (attribute)\|	439698008 \|Hereditary thrombophilia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (668539029) - 307091009 -> 281833003 (363698007) View
363698007 \|Finding site (attribute)\|	281833003 \|Entire hematological system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
439698008 View
439698008	Hereditary thrombophilia (disorder)	Primary thrombophilia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
307115002 View
307115002	Homozygous factor v leiden mutation (disorder)	Homozygous factor v leiden mutation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
307116001 View
307116001	Heterozygous factor v leiden mutation (disorder)	Đột biến yếu tố v leiden dị hợp tử	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 (71525f76-f23d-5d28-b4e5-454f20bb5aec) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D68.5	TRUE	ALWAYS D68.5	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 (9d28a027-b586-5ecd-847b-d321ff793cde) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D68.2	TRUE	ALWAYS D68.2	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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