dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 76642003

Production

add

Component

76642003

The component that hold information about this concept.

Fully Specified Name (FSN)

Factor x deficiency (disorder)

Shortest Term

Factor x deficiency

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 x deficiency (disorder)

SCTID: 76642003, Primitive, Active

76642003|Factor x deficiency (disorder)|

en Factor 10 deficiency
en Stuart-prower factor deficiency
en Factor x deficiency
en Factor x deficiency (disorder)

Expression

76642003 |Factor x deficiency (disorder)|
 <<< 234454002 |Prothrombin complex deficiency (disorder)| + 
86075001 |Coagulation factor deficiency syndrome (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
3036019012 - Factor 10 deficiency (en) View
3036019012	en	Synonym (core metadata concept)	Factor 10 deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1234012018 - Stuart-Prower factor deficiency (en) View
1234012018	en	Synonym (core metadata concept)	Stuart-Prower factor deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
127274011 - Factor X deficiency (en) View
127274011	en	Synonym (core metadata concept)	Factor X deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
817385017 - Factor X deficiency (disorder) (en) View
817385017	en	Fully specified name (core metadata concept)	Factor X deficiency (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
127275012 - Factor X deficiency, NOS (en) View
127275012	en	Synonym (core metadata concept)	Factor X deficiency, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11290540028) - 76642003 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11290541029) - 76642003 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2737294020) - 76642003 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2788754023) - 76642003 -> 128153000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	128153000 \|Hemostatic system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (865498022) - 76642003 -> 281833003 (363698007) View
363698007 \|Finding site (attribute)\|	281833003 \|Entire hematological system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (272600029) - 76642003 -> 234454002 (116680003) View
116680003 \|Is a (attribute)\|	234454002 \|Prothrombin complex deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (272601025) - 76642003 -> 86075001 (116680003) View
116680003 \|Is a (attribute)\|	86075001 \|Coagulation factor deficiency syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
86075001 View
86075001	Coagulation factor deficiency syndrome (disorder)	Coagulation factor disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234454002 View
234454002	Prothrombin complex deficiency (disorder)	Prothrombin complex deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1148862002 View
1148862002	Deficiency of factor x due to systemic amyloidosis (disorder)	Factor x deficiency due to systemic amyloidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
33820001 View
33820001	Acquired factor x deficiency disease (disorder)	Acquired factor x deficiency	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
37350004 View
37350004	Hereditary factor x deficiency disease (disorder)	Hereditary factor x deficiency disease	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 (a9d8f112-8cdd-5d01-be9b-d8cef3b66720) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D68.2	TRUE	ALWAYS D68.2 \| 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)\|

Terminology chevron_right Concepts chevron_right 76642003

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches