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Terminology chevron_right Concepts chevron_right 481462461000119102

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Component

481462461000119102

The component that hold information about this concept.

Fully Specified Name (FSN)

Carrier of spinal muscular atrophy (finding)

Shortest Term

Carrier of spinal muscular atrophy

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

Carrier of spinal muscular atrophy (finding)

SCTID: 481462461000119102, Primitive, Active

481462461000119102|Carrier of spinal muscular atrophy (finding)|

vi Người mang teo cơ tuỷ sống (phát hiện)
en Carrier of spinal muscular atrophy
en Carrier of spinal muscular atrophy (finding)

Expression

481462461000119102 |Carrier of spinal muscular atrophy (finding)|
 <<< 47461006 |Genetic disorder carrier (finding)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)| }
        { 363714003 |Interprets (attribute)| = 278844005 |General clinical state (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2006426 - Người mang teo cơ tuỷ sống (phát hiện) (vi) View
2006426	vi	Synonym (core metadata concept)	Người mang teo cơ tuỷ sống (phát hiện)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4024730018 - Carrier of spinal muscular atrophy (en) View
4024730018	en	Synonym (core metadata concept)	Carrier of spinal muscular atrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4024729011 - Carrier of spinal muscular atrophy (finding) (en) View
4024729011	en	Fully specified name (core metadata concept)	Carrier of spinal muscular atrophy (finding)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13035670028) - 481462461000119102 -> 47461006 (116680003) View
116680003 \|Is a (attribute)\|	47461006 \|Genetic disorder carrier (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13035671029) - 481462461000119102 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13035672020) - 481462461000119102 -> 278844005 (363714003) View
363714003 \|Interprets (attribute)\|	278844005 \|General clinical state (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
47461006 View
47461006	Genetic disorder carrier (finding)	Genetic disorder carrier	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 (99693ecb-efac-5b4a-9c9d-96975be345cc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

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