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Terminology chevron_right Concepts chevron_right 85672005

Production

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Component

85672005

The component that hold information about this concept.

Fully Specified Name (FSN)

Anterior horn cell disease (disorder)

Shortest Term

Bệnh tế bào sừng trước

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

Anterior horn cell disease (disorder)

SCTID: 85672005, Primitive, Active

85672005|Anterior horn cell disease (disorder)|

vi Bệnh tế bào sừng trước
en Anterior horn cell disease
en Anterior horn cell disease (disorder)

Expression

85672005 |Anterior horn cell disease (disorder)|
 <<< 84590007 |Lower motor neuron disease (disorder)| : 
        { 363698007 |Finding site (attribute)| = 25087005 |Structure of nervous system (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
502831000003118 - bệnh tế bào sừng trước (vi) View
502831000003118	vi	Synonym (core metadata concept)	bệnh tế bào sừng trước	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
142016013 - Anterior horn cell disease (en) View
142016013	en	Synonym (core metadata concept)	Anterior horn cell disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
827775019 - Anterior horn cell disease (disorder) (en) View
827775019	en	Fully specified name (core metadata concept)	Anterior horn cell disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
142017016 - Anterior horn cell disease, NOS (en) View
142017016	en	Synonym (core metadata concept)	Anterior horn cell disease, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2270716020) - 85672005 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (287746022) - 85672005 -> 230244008 (116680003) View
116680003 \|Is a (attribute)\|	230244008 \|Disorder primarily affecting the motor pathways (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (564925025) - 85672005 -> 31513005 (363698007) View
363698007 \|Finding site (attribute)\|	31513005 \|Motor neuron (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (564924026) - 85672005 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (287745021) - 85672005 -> 84590007 (116680003) View
116680003 \|Is a (attribute)\|	84590007 \|Lower motor neuron disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
84590007 View
84590007	Lower motor neuron disease (disorder)	Lower motor neuron disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
715565004 View
715565004	Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder)	Vuopala disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
64383006 View
64383006	Werdnig-hoffmann disease (disorder)	Werdnig-hoffmann disease	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 (ac588d0d-dd97-505c-9789-dfb1d11d4567) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G12.0	IFA 64383006 \| Werdnig-Hoffmann disease (disorder) \|	IF WERDNIG-HOFFMANN DISEASE CHOOSE G12.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (d0f87c18-28d7-5049-815b-3543efa44788) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G12.2	TRUE	ALWAYS G12.2	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 (e750c9e0-7be0-5e2c-af16-3c9e26c057b1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G12.2	OTHERWISE TRUE	ALWAYS G12.2	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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