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Terminology chevron_right Concepts chevron_right 95845002

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Component

95845002

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary dysplasminogenemia (disorder)

Shortest Term

Hereditary dysplasminogenemia

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

Hereditary dysplasminogenemia (disorder)

SCTID: 95845002, Primitive, Active

95845002|Hereditary dysplasminogenemia (disorder)|

en Hereditary dysfunctional plasminogen
en Hereditary dysplasminogenaemia
en Hereditary dysplasminogenemia
en Hereditary dysplasminogenemia (disorder)

Expression

95845002 |Hereditary dysplasminogenemia (disorder)|
 <<< 95844003 |Dysplasminogenemia (disorder)| + 
32895009 |Hereditary disease (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
158747012 - Hereditary dysfunctional plasminogen (en) View
158747012	en	Synonym (core metadata concept)	Hereditary dysfunctional plasminogen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
512327017 - Hereditary dysplasminogenaemia (en) View
512327017	en	Synonym (core metadata concept)	Hereditary dysplasminogenaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
158745016 - Hereditary dysplasminogenemia (en) View
158745016	en	Synonym (core metadata concept)	Hereditary dysplasminogenemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
840084015 - Hereditary dysplasminogenemia (disorder) (en) View
840084015	en	Fully specified name (core metadata concept)	Hereditary dysplasminogenemia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11290474026) - 95845002 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11290475025) - 95845002 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2699304024) - 95845002 -> 363137000 (116680003) View
116680003 \|Is a (attribute)\|	363137000 \|Hereditary disorder by system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2740031022) - 95845002 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2789436028) - 95845002 -> 128153000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	128153000 \|Hemostatic system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3499858028) - 95845002 -> 32895009 (116680003) View
116680003 \|Is a (attribute)\|	32895009 \|Hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (307956026) - 95845002 -> 363136009 (116680003) View
116680003 \|Is a (attribute)\|	363136009 \|Hereditary disorder of hematologic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (931126022) - 95845002 -> 281833003 (363698007) View
363698007 \|Finding site (attribute)\|	281833003 \|Entire hematological system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (307955027) - 95845002 -> 95844003 (116680003) View
116680003 \|Is a (attribute)\|	95844003 \|Dysplasminogenemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
32895009 View
32895009	Hereditary disease (disorder)	Genetic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
95844003 View
95844003	Dysplasminogenemia (disorder)	Dysplasminogenemia	900000000000074008 \|Necessary but not sufficient concept 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 (3be26942-51c2-52a6-8a70-5e11ede245c6) 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)\|

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