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Terminology chevron_right Concepts chevron_right 230437002

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Component

230437002

The component that hold information about this concept.

Fully Specified Name (FSN)

Dravet syndrome (disorder)

Shortest Term

Dravet syndrome

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

Dravet syndrome (disorder)

SCTID: 230437002, Primitive, Active

230437002|Dravet syndrome (disorder)|

en Dravet syndrome
en Dravet syndrome (disorder)
en Ds - dravet syndrome

Expression

230437002 |Dravet syndrome (disorder)|
 <<< 1275631007 |Developmental and epileptic encephalopathy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)|,
246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5373650013 - Dravet syndrome (en) View
5373650013	en	Synonym (core metadata concept)	Dravet syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3513043019 - Dravet Syndrome (en) View
3513043019	en	Synonym (core metadata concept)	Dravet Syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
5373651012 - Dravet syndrome (disorder) (en) View
5373651012	en	Fully specified name (core metadata concept)	Dravet syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
5373652017 - DS - Dravet syndrome (en) View
5373652017	en	Synonym (core metadata concept)	DS - Dravet syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
345311015 - Severe myoclonic epilepsy in infancy (en) View
345311015	en	Synonym (core metadata concept)	Severe myoclonic epilepsy in infancy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False
618244013 - Severe myoclonic epilepsy in infancy (disorder) (en) View
618244013	en	Fully specified name (core metadata concept)	Severe myoclonic epilepsy in infancy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7165905025) - 230437002 -> 698762005 (116680003) View
116680003 \|Is a (attribute)\|	698762005 \|Refractory myoclonic epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7165906029) - 230437002 -> 723125008 (116680003) View
116680003 \|Is a (attribute)\|	723125008 \|Epileptic encephalopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7165908028) - 230437002 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15609664024) - 230437002 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15627470022) - 230437002 -> 1275631007 (116680003) View
116680003 \|Is a (attribute)\|	1275631007 \|Developmental and epileptic encephalopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15627471021) - 230437002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13882802022) - 230437002 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2252849029) - 230437002 -> 91175000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	91175000 \|Seizure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (491349020) - 230437002 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1654139022) - 230437002 -> 230412007 (116680003) View
116680003 \|Is a (attribute)\|	230412007 \|Myoclonic epilepsy of early childhood (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1724464025) - 230437002 -> 255398004 (246454002) View
246454002 \|Occurrence (attribute)\|	255398004 \|Childhood (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1724465029) - 230437002 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7165907022) - 230437002 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (491348028) - 230437002 -> 24484000 (246112005) View
246112005 \|Severity (attribute)\|	24484000 \|Severe (severity modifier) (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (40845028) - 230437002 -> 230435005 (116680003) View
116680003 \|Is a (attribute)\|	230435005 \|Epilepsy undetermined whether focal or generalized (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1275631007 View
1275631007	Developmental and epileptic encephalopathy (disorder)	Developmental and epileptic encephalopathy	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 (585e5a1e-87be-53c9-8e9e-000ff8c61639) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G40.4	TRUE	ALWAYS G40.4 \| 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)\|
ExtendedMap object (75a864aa-5365-54fc-a11a-5ac1c61a26ff) 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)\|

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