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Terminology chevron_right Concepts chevron_right 472825005

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Component

472825005

The component that hold information about this concept.

Fully Specified Name (FSN)

Fetal chromosomal abnormality screening (procedure)

Shortest Term

Fetal chromosomal abnormality screening

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

Fetal chromosomal abnormality screening (procedure)

SCTID: 472825005, Primitive, Active

472825005|Fetal chromosomal abnormality screening (procedure)|

en Fetal chromosomal abnormality screening
en Fetal chromosomal abnormality screening (procedure)
en Foetal chromosomal abnormality screening

Expression

472825005 |Fetal chromosomal abnormality screening (procedure)|
 <<< 171242005 |Chromosome abnormality screening (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
2951931014 - Fetal chromosomal abnormality screening (en) View
2951931014	en	Synonym (core metadata concept)	Fetal chromosomal abnormality screening	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2951938015 - Fetal chromosomal abnormality screening (procedure) (en) View
2951938015	en	Fully specified name (core metadata concept)	Fetal chromosomal abnormality screening (procedure)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2951925011 - Foetal chromosomal abnormality screening (en) View
2951925011	en	Synonym (core metadata concept)	Foetal chromosomal abnormality screening	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4678586027) - 472825005 -> 360156006 (363703001) View
363703001 \|Has intent (attribute)\|	360156006 \|Screening - procedure intent (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16059733021) - 472825005 -> 360156006 (363703001) View
363703001 \|Has intent (attribute)\|	360156006 \|Screening - procedure intent (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4678585028) - 472825005 -> 129265001 (260686004) View
260686004 \|Method (attribute)\|	129265001 \|Evaluation - action (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4678587020) - 472825005 -> 409709004 (363702006) View
363702006 \|Has focus (attribute)\|	409709004 \|Chromosomal disorder (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4678584029) - 472825005 -> 171242005 (116680003) View
116680003 \|Is a (attribute)\|	171242005 \|Chromosome abnormality screening (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
171242005 View
171242005	Chromosome abnormality screening (procedure)	Chromosome abnormality screening	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

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