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Terminology chevron_right Concepts chevron_right 717942003

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Component

717942003

The component that hold information about this concept.

Fully Specified Name (FSN)

Brain dopamine-serotonin vesicular transport disease (disorder)

Shortest Term

Brain dopamine-serotonin vesicular transport disease

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

Brain dopamine-serotonin vesicular transport disease (disorder)

SCTID: 717942003, Primitive, Active

717942003|Brain dopamine-serotonin vesicular transport disease (disorder)|

en Brain dopamine-serotonin vesicular transport disease
en Brain dopamine-serotonin vesicular transport disease (disorder)

Expression

717942003 |Brain dopamine-serotonin vesicular transport disease (disorder)|
 <<< 15802004 |Dystonia (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
111394006 |Metabolic disorder of transport (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| : 
        { 363698007 |Finding site (attribute)| = 76375004 |Extrapyramidal system structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3324412015 - Brain dopamine-serotonin vesicular transport disease (en) View
3324412015	en	Synonym (core metadata concept)	Brain dopamine-serotonin vesicular transport disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3324411010 - Brain dopamine-serotonin vesicular transport disease (disorder) (en) View
3324411010	en	Fully specified name (core metadata concept)	Brain dopamine-serotonin vesicular transport disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13882867025) - 717942003 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16350699021) - 717942003 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6760027025) - 717942003 -> 76375004 (363698007) View
363698007 \|Finding site (attribute)\|	76375004 \|Extrapyramidal system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6760023026) - 717942003 -> 15802004 (116680003) View
116680003 \|Is a (attribute)\|	15802004 \|Dystonia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6760024021) - 717942003 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6760025022) - 717942003 -> 111394006 (116680003) View
116680003 \|Is a (attribute)\|	111394006 \|Metabolic disorder of transport (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6760026023) - 717942003 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
15802004 View
15802004	Dystonia (disorder)	Dystonia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
111394006 View
111394006	Metabolic disorder of transport (disorder)	Metabolic disorder of transport	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	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 (62720eff-cd8e-5ad9-81a0-a759c2735b1f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G25.8	TRUE	ALWAYS G25.8 \| 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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