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Terminology chevron_right Concepts chevron_right 230389006

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Component

230389006

The component that hold information about this concept.

Fully Specified Name (FSN)

Primary inherited reading epilepsy (disorder)

Shortest Term

Primary inherited reading 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

Primary inherited reading epilepsy (disorder)

SCTID: 230389006, Primitive, Active

230389006|Primary inherited reading epilepsy (disorder)|

en Primary inherited reading epilepsy
en Primary inherited reading epilepsy (disorder)

Expression

230389006 |Primary inherited reading epilepsy (disorder)|
 <<< 79745005 |Reflex epilepsy (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
1260117009 |Combined focal and generalized epilepsy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
345238013 - Primary inherited reading epilepsy (en) View
345238013	en	Synonym (core metadata concept)	Primary inherited reading epilepsy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
618190011 - Primary inherited reading epilepsy (disorder) (en) View
618190011	en	Fully specified name (core metadata concept)	Primary inherited reading epilepsy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (491223028) - 230389006 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15592139022) - 230389006 -> 1260117009 (116680003) View
116680003 \|Is a (attribute)\|	1260117009 \|Combined focal and generalized epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15592182023) - 230389006 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (40782027) - 230389006 -> 278510009 (116680003) View
116680003 \|Is a (attribute)\|	278510009 \|Localization-related idiopathic epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12252227022) - 230389006 -> 79745005 (116680003) View
116680003 \|Is a (attribute)\|	79745005 \|Reflex epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12252228028) - 230389006 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2252805026) - 230389006 -> 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
1260117009 View
1260117009	Combined focal and generalized epilepsy (disorder)	Combined focal and generalised epilepsy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
79745005 View
79745005	Reflex epilepsy (disorder)	Reflex epilepsy	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 (852fba0e-d784-5923-b53c-e5582df0dc2e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G40.0	TRUE	ALWAYS G40.0	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 230389006

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