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Terminology chevron_right Concepts chevron_right 230422001

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Component

230422001

The component that hold information about this concept.

Fully Specified Name (FSN)

Epilepsy with myoclonic absence (disorder)

Shortest Term

Myoclonic absence 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

Epilepsy with myoclonic absence (disorder)

SCTID: 230422001, Primitive, Active

230422001|Epilepsy with myoclonic absence (disorder)|

en Ema - epilepsy with myoclonic absence
en Epilepsy with myoclonic absence
en Epilepsy with myoclonic absence (disorder)
en Myoclonic absence epilepsy

Expression

230422001 |Epilepsy with myoclonic absence (disorder)|
 <<< 1260407007 |Genetic generalized epilepsy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)|,
246454002 |Occurrence (attribute)| = 255398004 |Childhood (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5173086013 - EMA - epilepsy with myoclonic absence (en) View
5173086013	en	Synonym (core metadata concept)	EMA - epilepsy with myoclonic absence	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
5173085012 - Epilepsy with myoclonic absence (en) View
5173085012	en	Synonym (core metadata concept)	Epilepsy with myoclonic absence	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5173084011 - Epilepsy with myoclonic absence (disorder) (en) View
5173084011	en	Fully specified name (core metadata concept)	Epilepsy with myoclonic absence (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
345287010 - Epilepsy with myoclonic absences (en) View
345287010	en	Synonym (core metadata concept)	Epilepsy with myoclonic absences	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
618227014 - Myoclonic absence epilepsy (disorder) (en) View
618227014	en	Fully specified name (core metadata concept)	Myoclonic absence epilepsy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False
345288017 - Myoclonic absence epilepsy (en) View
345288017	en	Synonym (core metadata concept)	Myoclonic absence epilepsy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (491272024) - 230422001 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13672046021) - 230422001 -> 19598007 (116680003) View
116680003 \|Is a (attribute)\|	19598007 \|Generalized epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15295240027) - 230422001 -> 1208629005 (116680003) View
116680003 \|Is a (attribute)\|	1208629005 \|Myoclonic absence seizure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15514495028) - 230422001 -> 1260407007 (116680003) View
116680003 \|Is a (attribute)\|	1260407007 \|Genetic generalized epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15514496027) - 230422001 -> 255398004 (246454002) View
246454002 \|Occurrence (attribute)\|	255398004 \|Childhood (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15611994021) - 230422001 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13672045020) - 230422001 -> 79631006 (116680003) View
116680003 \|Is a (attribute)\|	79631006 \|Absence seizure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (40823029) - 230422001 -> 230415009 (116680003) View
116680003 \|Is a (attribute)\|	230415009 \|Cryptogenic generalized epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2252835022) - 230422001 -> 91175000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	91175000 \|Seizure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1260407007 View
1260407007	Genetic generalized epilepsy (disorder)	Genetic generalised 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 (298e8689-0acc-596a-8cb5-5c74f6837852) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G40.4	TRUE	ALWAYS G40.4	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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