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Terminology chevron_right Concepts chevron_right 171242005

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Component

171242005

The component that hold information about this concept.

Fully Specified Name (FSN)

Chromosome abnormality screening (procedure)

Shortest Term

Chromosome abnormality screening

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Chromosome abnormality screening (procedure)

SCTID: 171242005, Defined, Active

171242005|Chromosome abnormality screening (procedure)|

en Chromosome abnormality screening
en Chromosome abnormality screening (procedure)

Expression

171242005 |Chromosome abnormality screening (procedure)|
 === 312851005 |Screening for disorder (procedure)| : 
        { 363703001 |Has intent (attribute)| = 360156006 |Screening - procedure intent (qualifier value)|,
260686004 |Method (attribute)| = 129265001 |Evaluation - action (qualifier value)| }
        { 363702006 |Has focus (attribute)| = 409709004 |Chromosomal disorder (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
265342018 - Chromosome abnormality screening (en) View
265342018	en	Synonym (core metadata concept)	Chromosome abnormality screening	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
553282019 - Chromosome abnormality screening (procedure) (en) View
553282019	en	Fully specified name (core metadata concept)	Chromosome abnormality screening (procedure)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (941234024) - 171242005 -> 360156006 (363703001) View
363703001 \|Has intent (attribute)\|	360156006 \|Screening - procedure intent (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16059731023) - 171242005 -> 360156006 (363703001) View
363703001 \|Has intent (attribute)\|	360156006 \|Screening - procedure intent (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3233531023) - 171242005 -> 409709004 (363702006) View
363702006 \|Has focus (attribute)\|	409709004 \|Chromosomal disorder (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3585626024) - 171242005 -> 129265001 (260686004) View
260686004 \|Method (attribute)\|	129265001 \|Evaluation - action (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (941233029) - 171242005 -> 64572001 (363702006) View
363702006 \|Has focus (attribute)\|	64572001 \|Disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (320092024) - 171242005 -> 312851005 (116680003) View
116680003 \|Is a (attribute)\|	312851005 \|Screening for disorder (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
312851005 View
312851005	Screening for disorder (procedure)	Screening for disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
472825005 View
472825005	Fetal chromosomal abnormality screening (procedure)	Fetal chromosomal abnormality screening	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
315115008 View
315115008	Downs screening test (procedure)	Downs screening test	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

Terminology chevron_right Concepts chevron_right 171242005

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