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Terminology chevron_right Concepts chevron_right 168118008

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Component

168118008

The component that hold information about this concept.

Fully Specified Name (FSN)

Trisomy 21 in amniotic fetal cell (finding)

Shortest Term

Amniotic fetal cell: mongol

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

Trisomy 21 in amniotic fetal cell (finding)

SCTID: 168118008, Primitive, Active

168118008|Trisomy 21 in amniotic fetal cell (finding)|

vi Phát hiện tam nhiễm sắc thể 21 trong tế bào ối (phát hiện)
en Trisomy 21 in amniotic fetal cell
en Trisomy 21 in amniotic fetal cell (finding)
en Trisomy 21 in amniotic foetal cell

Expression

168118008 |Trisomy 21 in amniotic fetal cell (finding)|
 <<< 168117003 |Amniotic fetal cell abnormal (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
2033444 - Phát hiện tam nhiễm sắc thể 21 trong tế bào ối (phát hiện) (vi) View
2033444	vi	Synonym (core metadata concept)	Phát hiện tam nhiễm sắc thể 21 trong tế bào ối (phát hiện)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2816401010 - Trisomy 21 in amniotic fetal cell (en) View
2816401010	en	Synonym (core metadata concept)	Trisomy 21 in amniotic fetal cell	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2816403013 - Trisomy 21 in amniotic fetal cell (finding) (en) View
2816403013	en	Fully specified name (core metadata concept)	Trisomy 21 in amniotic fetal cell (finding)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2816402015 - Trisomy 21 in amniotic foetal cell (en) View
2816402015	en	Synonym (core metadata concept)	Trisomy 21 in amniotic foetal cell	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
261108013 - Amniotic fetal cell: mongol (en) View
261108013	en	Synonym (core metadata concept)	Amniotic fetal cell: mongol	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
549805013 - Amniotic fetal cell: mongol (finding) (en) View
549805013	en	Fully specified name (core metadata concept)	Amniotic fetal cell: mongol (finding)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3610115021) - 168118008 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3610116022) - 168118008 -> 168115006 (363714003) View
363714003 \|Interprets (attribute)\|	168115006 \|Amniotic fetal cell study (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3662150020) - 168118008 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3662151024) - 168118008 -> 168115006 (363714003) View
363714003 \|Interprets (attribute)\|	168115006 \|Amniotic fetal cell study (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (318190029) - 168118008 -> 365841001 (116680003) View
116680003 \|Is a (attribute)\|	365841001 \|Body substance analysis finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (938507027) - 168118008 -> 271919007 (363714003) View
363714003 \|Interprets (attribute)\|	271919007 \|Body substance analysis interpretation (observable entity)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2790951022) - 168118008 -> 15220000 (363714003) View
363714003 \|Interprets (attribute)\|	15220000 \|Laboratory test (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3564917024) - 168118008 -> 168117003 (116680003) View
116680003 \|Is a (attribute)\|	168117003 \|Amniotic fetal cell abnormal (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2874159020) - 168118008 -> 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
168117003 View
168117003	Amniotic fetal cell abnormal (finding)	Amniotic fetal cell abnormal	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 (3526cd6f-8b42-5c33-8eaf-29e009540ace) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	O28.5	TRUE	ALWAYS O28.5	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)\|

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