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Terminology chevron_right Concepts chevron_right 254262003

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Component

254262003

The component that hold information about this concept.

Fully Specified Name (FSN)

Unbalanced translocation and insertion (disorder)

Shortest Term

Unbalanced translocation and insertion

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

Unbalanced translocation and insertion (disorder)

SCTID: 254262003, Primitive, Active

254262003|Unbalanced translocation and insertion (disorder)|

en Unbalanced translocation and insertion
en Unbalanced translocation and insertion (disorder)

Expression

254262003 |Unbalanced translocation and insertion (disorder)|
 <<< 409709004 |Chromosomal disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 15897004 |Chromosomal translocation (morphologic abnormality)| }
        { 363698007 |Finding site (attribute)| = 312237004 |Chromosome structure (cell structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
378492015 - Unbalanced translocation and insertion (en) View
378492015	en	Synonym (core metadata concept)	Unbalanced translocation and insertion	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
645130015 - Unbalanced translocation and insertion (disorder) (en) View
645130015	en	Fully specified name (core metadata concept)	Unbalanced translocation and insertion (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3784685026) - 254262003 -> 15897004 (116676008) View
116676008 \|Associated morphology (attribute)\|	15897004 \|Chromosomal translocation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5033430022) - 254262003 -> 312237004 (363698007) View
363698007 \|Finding site (attribute)\|	312237004 \|Chromosome structure (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (74399029) - 254262003 -> 270521004 (116680003) View
116680003 \|Is a (attribute)\|	270521004 \|Trisomy and partial trisomy of autosome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (580269029) - 254262003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3393639026) - 254262003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3776338020) - 254262003 -> 409709004 (116680003) View
116680003 \|Is a (attribute)\|	409709004 \|Chromosomal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3393640029) - 254262003 -> 312237004 (363698007) View
363698007 \|Finding site (attribute)\|	312237004 \|Chromosome structure (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2579177026) - 254262003 -> 312237004 (363698007) View
363698007 \|Finding site (attribute)\|	312237004 \|Chromosome structure (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2579178020) - 254262003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (580270028) - 254262003 -> 41669009 (116676008) View
116676008 \|Associated morphology (attribute)\|	41669009 \|Alteration of chromosome structure (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
409709004 View
409709004	Chromosomal disorder (disorder)	Chromosomal anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
371045000 View
371045000	Translocation down syndrome (disorder)	Translocation down syndrome	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
ExtendedMap object (b8c9f5f8-9082-584d-93a7-37905447d9b5) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q99.8	TRUE	ALWAYS Q99.8	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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