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Terminology chevron_right Concepts chevron_right 770405003

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Component

770405003

The component that hold information about this concept.

Fully Specified Name (FSN)

Benign familial mesial temporal lobe epilepsy (disorder)

Shortest Term

Familial mesial temporal lobe 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

Benign familial mesial temporal lobe epilepsy (disorder)

SCTID: 770405003, Primitive, Active

770405003|Benign familial mesial temporal lobe epilepsy (disorder)|

en Familial mesial temporal lobe epilepsy
en Familial mesial temporal lobe epilepsy (disorder)
en Fmtle - familial mesial temporal lobe epilepsy
en Benign familial mesial temporal lobe epilepsy

Expression

770405003 |Benign familial mesial temporal lobe epilepsy (disorder)|
 <<< 363235000 |Hereditary disorder of nervous system (disorder)| + 
783739005 |Familial temporal lobe epilepsy (disorder)| + 
1343664003 |Mesial temporal lobe epilepsy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 78277001 |Temporal lobe structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3700716012 - Benign familial mesial temporal lobe epilepsy (disorder) (en) View
3700716012	en	Fully specified name (core metadata concept)	Benign familial mesial temporal lobe epilepsy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False
3700715011 - Benign FMTLE (familial mesial temporal lobe epilepsy) (en) View
3700715011	en	Synonym (core metadata concept)	Benign FMTLE (familial mesial temporal lobe epilepsy)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
5362253014 - Familial mesial temporal lobe epilepsy (en) View
5362253014	en	Synonym (core metadata concept)	Familial mesial temporal lobe epilepsy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5362254015 - Familial mesial temporal lobe epilepsy (disorder) (en) View
5362254015	en	Fully specified name (core metadata concept)	Familial mesial temporal lobe epilepsy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5362252016 - FMTLE - familial mesial temporal lobe epilepsy (en) View
5362252016	en	Synonym (core metadata concept)	FMTLE - familial mesial temporal lobe epilepsy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3700714010 - Benign familial mesial temporal lobe epilepsy (en) View
3700714010	en	Synonym (core metadata concept)	Benign familial mesial temporal lobe epilepsy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16169997026) - 770405003 -> 1343664003 (116680003) View
116680003 \|Is a (attribute)\|	1343664003 \|Mesial temporal lobe epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619281029) - 770405003 -> 193000002 (116680003) View
116680003 \|Is a (attribute)\|	193000002 \|Temporal lobe epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9619282020) - 770405003 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16024575020) - 770405003 -> 783739005 (116680003) View
116680003 \|Is a (attribute)\|	783739005 \|Familial temporal lobe epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619284021) - 770405003 -> 78277001 (363698007) View
363698007 \|Finding site (attribute)\|	78277001 \|Temporal lobe structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619283026) - 770405003 -> 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
1343664003 View
1343664003	Mesial temporal lobe epilepsy (disorder)	Mesial temporal lobe epilepsy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
783739005 View
783739005	Familial temporal lobe epilepsy (disorder)	Familial temporal lobe 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 (1a352554-fa39-57b3-a724-9bbaacae5c8c) 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)\|
ExtendedMap object (5cfc3812-8042-5531-a35b-6c127fd7cfcc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G40.2	TRUE	ALWAYS G40.2	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 770405003

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