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Terminology chevron_right Concepts chevron_right 253185002

Production

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Component

253185002

The component that hold information about this concept.

Fully Specified Name (FSN)

Chiari malformation type i (disorder)

Shortest Term

Dị tật chiari loại i

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

Chiari malformation type i (disorder)

SCTID: 253185002, Primitive, Active

253185002|Chiari malformation type i (disorder)|

vi Dị tật chiari loại i
en Arnold chiari type 1
en Chiari malformation type i (disorder)
en Chiari malformation type i

Expression

253185002 |Chiari malformation type i (disorder)|
 <<< 253184003 |Chiari malformation (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 414403008 |Herniated structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 113305005 |Cerebellar structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
571391000003113 - dị tật Chiari loại I (vi) View
571391000003113	vi	Synonym (core metadata concept)	dị tật Chiari loại I	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2966580013 - Arnold Chiari type 1 (en) View
2966580013	en	Synonym (core metadata concept)	Arnold Chiari type 1	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
643914014 - Chiari malformation type I (disorder) (en) View
643914014	en	Fully specified name (core metadata concept)	Chiari malformation type I (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
377081010 - Chiari malformation type I (en) View
377081010	en	Synonym (core metadata concept)	Chiari malformation type I	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (568617024) - 253185002 -> 280369009 (363698007) View
363698007 \|Finding site (attribute)\|	280369009 \|Brain tissue structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3414582024) - 253185002 -> 414403008 (116676008) View
116676008 \|Associated morphology (attribute)\|	414403008 \|Herniated structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3453687027) - 253185002 -> 4919007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4919007 \|Congenital protrusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11355019025) - 253185002 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4980862029) - 253185002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5017568025) - 253185002 -> 4919007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4919007 \|Congenital protrusion (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5017569022) - 253185002 -> 280369009 (363698007) View
363698007 \|Finding site (attribute)\|	280369009 \|Brain tissue structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6125416026) - 253185002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517344029) - 253185002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (568618025) - 253185002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3467376029) - 253185002 -> 280369009 (363698007) View
363698007 \|Finding site (attribute)\|	280369009 \|Brain tissue structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2715381025) - 253185002 -> 4919007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4919007 \|Congenital protrusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2715382021) - 253185002 -> 414403008 (116676008) View
116676008 \|Associated morphology (attribute)\|	414403008 \|Herniated structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2578741023) - 253185002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (73025027) - 253185002 -> 253184003 (116680003) View
116680003 \|Is a (attribute)\|	253184003 \|Chiari malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
253184003 View
253184003	Chiari malformation (disorder)	Dị tật chiari	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
720815000 View
720815000	Capra demarco syndrome (disorder)	Berant 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 (2304ee3f-16d4-5f5c-9ca2-6808864c4765) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q07.0	TRUE	ALWAYS Q07.0	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)\|
ExtendedMap object (befedeba-ec06-5ac9-b73b-62f120b2bccc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q07.8	TRUE	ALWAYS Q07.8	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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