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Terminology chevron_right Concepts chevron_right 168117003

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Component

168117003

The component that hold information about this concept.

Fully Specified Name (FSN)

Amniotic fetal cell abnormal (finding)

Shortest Term

Amniotic fetal cell abnormal

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

Amniotic fetal cell abnormal (finding)

SCTID: 168117003, Primitive, Active

168117003|Amniotic fetal cell abnormal (finding)|

vi Tế bào thai nước ối bất thường (phát hiện)
en Amniotic fetal cell abnormal
en Amniotic fetal cell abnormal (finding)
en Amniotic foetal cell abnormal

Expression

168117003 |Amniotic fetal cell abnormal (finding)|
 <<< 309198006 |Abnormal histology findings (finding)| : 
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 168115006 |Amniotic fetal cell study (procedure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2003584 - Tế bào thai nước ối bất thường (phát hiện) (vi) View
2003584	vi	Synonym (core metadata concept)	Tế bào thai nước ối bất thường (phát hiện)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
261107015 - Amniotic fetal cell abnormal (en) View
261107015	en	Synonym (core metadata concept)	Amniotic fetal cell abnormal	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
549804012 - Amniotic fetal cell abnormal (finding) (en) View
549804012	en	Fully specified name (core metadata concept)	Amniotic fetal cell abnormal (finding)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2819580011 - Amniotic foetal cell abnormal (en) View
2819580011	en	Synonym (core metadata concept)	Amniotic foetal cell abnormal	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3602619025) - 168117003 -> 168115006 (363714003) View
363714003 \|Interprets (attribute)\|	168115006 \|Amniotic fetal cell study (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3610114020) - 168117003 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3661850021) - 168117003 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3688113024) - 168117003 -> 168115006 (363714003) View
363714003 \|Interprets (attribute)\|	168115006 \|Amniotic fetal cell study (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (318189022) - 168117003 -> 309196005 (116680003) View
116680003 \|Is a (attribute)\|	309196005 \|Abnormal cytology findings (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2790950023) - 168117003 -> 15220000 (363714003) View
363714003 \|Interprets (attribute)\|	15220000 \|Laboratory test (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3574956025) - 168117003 -> 309198006 (116680003) View
116680003 \|Is a (attribute)\|	309198006 \|Abnormal histology findings (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2874158028) - 168117003 -> 71388002 (418775008) View
418775008 \|Finding method (attribute)\|	71388002 \|Procedure (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
309198006 View
309198006	Abnormal histology findings (finding)	Histology abnormal	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
168118008 View
168118008	Trisomy 21 in amniotic fetal cell (finding)	Amniotic fetal cell: mongol	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 (d6a17ef1-35d9-59d8-83ea-4f121a83129f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	O28.2	TRUE	ALWAYS O28.2	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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