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Terminology chevron_right Concepts chevron_right 230423006

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Component

230423006

The component that hold information about this concept.

Fully Specified Name (FSN)

Unverricht-lundborg syndrome (disorder)

Shortest Term

Baltic myoclonus epilepsy

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

Unverricht-lundborg syndrome (disorder)

SCTID: 230423006, Primitive, Active

230423006|Unverricht-lundborg syndrome (disorder)|

en Unverricht-lundborg syndrome (disorder)
en Baltic myoclonus epilepsy
en Unverricht-lundborg disease
en Unverricht-lundborg syndrome

Expression

230423006 |Unverricht-lundborg syndrome (disorder)|
 <<< 267581004 |Progressive myoclonic epilepsy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 83678007 |Cerebral structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
618228016 - Unverricht-Lundborg syndrome (disorder) (en) View
618228016	en	Fully specified name (core metadata concept)	Unverricht-Lundborg syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
345291017 - Baltic myoclonus epilepsy (en) View
345291017	en	Synonym (core metadata concept)	Baltic myoclonus epilepsy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
345290016 - Unverricht-Lundborg disease (en) View
345290016	en	Synonym (core metadata concept)	Unverricht-Lundborg disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
345289013 - Unverricht-Lundborg syndrome (en) View
345289013	en	Synonym (core metadata concept)	Unverricht-Lundborg syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13882785028) - 230423006 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (491273025) - 230423006 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2252836023) - 230423006 -> 91175000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	91175000 \|Seizure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (40824024) - 230423006 -> 267581004 (116680003) View
116680003 \|Is a (attribute)\|	267581004 \|Progressive myoclonic epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
267581004 View
267581004	Progressive myoclonic epilepsy (disorder)	Progressive myoclonic epilepsy	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 (ce6ab11d-190d-5584-a237-0a66600e1c02) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G40.3	TRUE	ALWAYS G40.3	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)\|

Terminology chevron_right Concepts chevron_right 230423006

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