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Tools chevron_right Concepts chevron_right 983888571000119106

Production

Component

983888571000119106

The component that hold information about this concept.

Fully Specified Name (FSN)

Carrier of walker-warburg congenital muscular dystrophy (finding)

Shortest Term

Carrier of walker-warburg congenital muscular dystrophy

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 walker-warburg congenital muscular dystrophy (finding)

SCTID: 983888571000119106, Primitive, Active

983888571000119106|Carrier of walker-warburg congenital muscular dystrophy (finding)|

en Carrier of walker-warburg congenital muscular dystrophy
en Carrier of walker-warburg congenital muscular dystrophy (finding)

Expression

983888571000119106 |Carrier of walker-warburg congenital muscular dystrophy (finding)|
 <<< 137511000119103 |Carrier of muscular dystrophy (finding)| : 
        { 363714003 |Interprets (attribute)| = 278844005 |General clinical state (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5479468011 - Carrier of Walker-Warburg congenital muscular dystrophy (en) View
5479468011	en	Synonym (core metadata concept)	Carrier of Walker-Warburg congenital muscular dystrophy	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
5479467018 - Carrier of Walker-Warburg congenital muscular dystrophy (finding) (en) View
5479467018	en	Fully specified name (core metadata concept)	Carrier of Walker-Warburg congenital muscular dystrophy (finding)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16434842026) - 983888571000119106 -> 137511000119103 (116680003) View
116680003 \|Is a (attribute)\|	137511000119103 \|Carrier of muscular dystrophy (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16434843020) - 983888571000119106 -> 278844005 (363714003) View
363714003 \|Interprets (attribute)\|	278844005 \|General clinical state (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16434844025) - 983888571000119106 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
137511000119103 View
137511000119103	Carrier of muscular dystrophy (finding)	Carrier of muscular dystrophy	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 (5834d334-7310-5092-9025-6e94f47edf06) 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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