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Terminology chevron_right Concepts chevron_right 1280009

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Component

1280009

The component that hold information about this concept.

Fully Specified Name (FSN)

Isologous chimera (disorder)

Shortest Term

Isologous chimera

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

Isologous chimera (disorder)

SCTID: 1280009, Primitive, Active

1280009|Isologous chimera (disorder)|

en Isologous chimera
en Isologous chimera (disorder)

Expression

1280009 |Isologous chimera (disorder)|
 <<< 2229005 |Chimera (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 312237004 |Chromosome structure (cell structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
474279010 - Isologous chimaera (en) View
474279010	en	Synonym (core metadata concept)	Isologous chimaera	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False
3255016 - Isologous chimera (en) View
3255016	en	Synonym (core metadata concept)	Isologous chimera	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
731950013 - Isologous chimera (disorder) (en) View
731950013	en	Fully specified name (core metadata concept)	Isologous chimera (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (696677026) - 1280009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3361833025) - 1280009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5008199027) - 1280009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5008200029) - 1280009 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5008201025) - 1280009 -> 312237004 (363698007) View
363698007 \|Finding site (attribute)\|	312237004 \|Chromosome structure (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3361834020) - 1280009 -> 312237004 (363698007) View
363698007 \|Finding site (attribute)\|	312237004 \|Chromosome structure (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2590478029) - 1280009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2590479021) - 1280009 -> 312237004 (363698007) View
363698007 \|Finding site (attribute)\|	312237004 \|Chromosome structure (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2460466027) - 1280009 -> 54900001 (116680003) View
116680003 \|Is a (attribute)\|	54900001 \|Monster (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2483483029) - 1280009 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2483482023) - 1280009 -> 41669009 (116676008) View
116676008 \|Associated morphology (attribute)\|	41669009 \|Alteration of chromosome structure (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (696676024) - 1280009 -> 303112003 (246454002) View
246454002 \|Occurrence (attribute)\|	303112003 \|Fetal period (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (696678020) - 1280009 -> 55460000 (363698007) View
363698007 \|Finding site (attribute)\|	55460000 \|Fetal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (162967027) - 1280009 -> 2229005 (116680003) View
116680003 \|Is a (attribute)\|	2229005 \|Chimera (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
2229005 View
2229005	Chimera (disorder)	Chimera	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 (d13b0b64-0652-50c9-92df-533193a0312a) 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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