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Terminology chevron_right Concepts chevron_right 1003909007

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Component

1003909007

The component that hold information about this concept.

Fully Specified Name (FSN)

Proximal duplication of chromosome 13 (disorder)

Shortest Term

Proximal duplication of chromosome 13

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

Proximal duplication of chromosome 13 (disorder)

SCTID: 1003909007, Primitive, Active

1003909007|Proximal duplication of chromosome 13 (disorder)|

en Proximal duplication of chromosome 13
en Proximal duplication of chromosome 13 (disorder)

Expression

1003909007 |Proximal duplication of chromosome 13 (disorder)|
 <<< 726352003 |Partial trisomy of chromosome 13 (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 133849008 |Partial trisomy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 55401003 |Chromosome pair 13 (cell structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4166946015 - Proximal duplication of chromosome 13 (en) View
4166946015	en	Synonym (core metadata concept)	Proximal duplication of chromosome 13	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4166945016 - Proximal duplication of chromosome 13 (disorder) (en) View
4166945016	en	Fully specified name (core metadata concept)	Proximal duplication of chromosome 13 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13192124025) - 1003909007 -> 726352003 (116680003) View
116680003 \|Is a (attribute)\|	726352003 \|Partial trisomy of chromosome 13 (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13192125029) - 1003909007 -> 55401003 (363698007) View
363698007 \|Finding site (attribute)\|	55401003 \|Chromosome pair 13 (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13192126028) - 1003909007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13192127021) - 1003909007 -> 133849008 (116676008) View
116676008 \|Associated morphology (attribute)\|	133849008 \|Partial trisomy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
726352003 View
726352003	Partial trisomy of chromosome 13 (disorder)	Duplication of chromosome 13	900000000000073002 \|Sufficiently defined by necessary conditions 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 (df391163-1ccb-5c56-a22d-de254ed50d81) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q91.7	TRUE	ALWAYS Q91.7	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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