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Terminology chevron_right Concepts chevron_right 128098009

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Component

128098009

The component that hold information about this concept.

Fully Specified Name (FSN)

Scott syndrome (disorder)

Shortest Term

Scott 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

Scott syndrome (disorder)

SCTID: 128098009, Primitive, Active

128098009|Scott syndrome (disorder)|

en Scott syndrome (disorder)
en Scott syndrome

Expression

128098009 |Scott syndrome (disorder)|
 <<< 128096008 |Hereditary platelet function disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 91689009 |Body system structure (body structure)| }
        { 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
732057011 - Scott syndrome (disorder) (en) View
732057011	en	Fully specified name (core metadata concept)	Scott syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
194692010 - Scott syndrome (en) View
194692010	en	Synonym (core metadata concept)	Scott syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11570393029) - 128098009 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12436799022) - 128098009 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4785919029) - 128098009 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11570394024) - 128098009 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (696880027) - 128098009 -> 16378004 (363698007) View
363698007 \|Finding site (attribute)\|	16378004 \|Platelet (cell structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2728421026) - 128098009 -> 250311007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250311007 \|Platelet finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2785828021) - 128098009 -> 128153000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	128153000 \|Hemostatic system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264148022) - 128098009 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (696881028) - 128098009 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (163122029) - 128098009 -> 128096008 (116680003) View
116680003 \|Is a (attribute)\|	128096008 \|Hereditary platelet function disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
128096008 View
128096008	Hereditary platelet function disorder (disorder)	Hereditary platelet function disorder	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 (317ad81c-3c57-5f1b-b6b5-3a00f5ee81c2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q89.8	TRUE	ALWAYS Q89.8	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 (86505808-1a10-538e-aed3-e8d356c30a20) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D69.1	TRUE	ALWAYS D69.1	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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