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Terminology chevron_right Concepts chevron_right 784341001

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Component

784341001

The component that hold information about this concept.

Fully Specified Name (FSN)

Amyotrophic lateral sclerosis type 4 (disorder)

Shortest Term

Amyotrophic lateral sclerosis type 4

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

Amyotrophic lateral sclerosis type 4 (disorder)

SCTID: 784341001, Primitive, Active

784341001|Amyotrophic lateral sclerosis type 4 (disorder)|

en Als4 - amyotrophic lateral sclerosis type 4
en Amyotrophic lateral sclerosis type 4
en Amyotrophic lateral sclerosis type 4 (disorder)
en Dhmn (distal hereditary motor neuropathy) with upper motor neuron signs

Expression

784341001 |Amyotrophic lateral sclerosis type 4 (disorder)|
 <<< 128283000 |Chronic nervous system disorder (disorder)| + 
86044005 |Amyotrophic lateral sclerosis (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 21483005 |Structure of central nervous system (body structure)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3763686015 - ALS4 - amyotrophic lateral sclerosis type 4 (en) View
3763686015	en	Synonym (core metadata concept)	ALS4 - amyotrophic lateral sclerosis type 4	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3763685016 - Amyotrophic lateral sclerosis type 4 (en) View
3763685016	en	Synonym (core metadata concept)	Amyotrophic lateral sclerosis type 4	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3763688019 - Amyotrophic lateral sclerosis type 4 (disorder) (en) View
3763688019	en	Fully specified name (core metadata concept)	Amyotrophic lateral sclerosis type 4 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3763687012 - dHMN (distal hereditary motor neuropathy) with upper motor neuron signs (en) View
3763687012	en	Synonym (core metadata concept)	dHMN (distal hereditary motor neuropathy) with upper motor neuron signs	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11373691028) - 784341001 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11373695021) - 784341001 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11373697029) - 784341001 -> 80690008 (116680003) View
116680003 \|Is a (attribute)\|	80690008 \|Degenerative disease of the central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094744028) - 784341001 -> 106018006 (116680003) View
116680003 \|Is a (attribute)\|	106018006 \|Hereditary degenerative disease of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094745027) - 784341001 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373692024) - 784341001 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373693025) - 784341001 -> 86044005 (116680003) View
116680003 \|Is a (attribute)\|	86044005 \|Amyotrophic lateral sclerosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373694020) - 784341001 -> 21483005 (363698007) View
363698007 \|Finding site (attribute)\|	21483005 \|Structure of central nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373698023) - 784341001 -> 128283000 (116680003) View
116680003 \|Is a (attribute)\|	128283000 \|Chronic nervous system disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11572986027) - 784341001 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
106018006 View
106018006	Hereditary degenerative disease of central nervous system (disorder)	Hereditary degenerative disease of central nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
86044005 View
86044005	Amyotrophic lateral sclerosis (disorder)	Lou gehrig's disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128283000 View
128283000	Chronic nervous system disorder (disorder)	Chronic nervous system disease	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 (66b19184-3be0-5e40-8b37-9dce2da27625) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G12.2	TRUE	ALWAYS G12.2 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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