dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 784377008

Production

add

Component

784377008

The component that hold information about this concept.

Fully Specified Name (FSN)

Autosomal dominant epilepsy with auditory features (disorder)

Shortest Term

Partial epilepsy with auditory aura

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

Autosomal dominant epilepsy with auditory features (disorder)

SCTID: 784377008, Primitive, Active

784377008|Autosomal dominant epilepsy with auditory features (disorder)|

en Familial epilepsy with auditory features
en Familial epilepsy with auditory features (disorder)
en Feaf - familial epilepsy with auditory features
en Autosomal dominant epilepsy with auditory features
en Autosomal dominant lateral temporal lobe epilepsy

Expression

784377008 |Autosomal dominant epilepsy with auditory features (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
1332158001 |Epilepsy with auditory features (disorder)| + 
783739005 |Familial 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
3763853017 - Autosomal dominant epilepsy with auditory features (disorder) (en) View
3763853017	en	Fully specified name (core metadata concept)	Autosomal dominant epilepsy with auditory features (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False
5380923012 - Familial epilepsy with auditory features (en) View
5380923012	en	Synonym (core metadata concept)	Familial epilepsy with auditory features	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5380924018 - Familial epilepsy with auditory features (disorder) (en) View
5380924018	en	Fully specified name (core metadata concept)	Familial epilepsy with auditory features (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5380925017 - FEAF - familial epilepsy with auditory features (en) View
5380925017	en	Synonym (core metadata concept)	FEAF - familial epilepsy with auditory features	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3763852010 - Partial epilepsy with auditory aura (en) View
3763852010	en	Synonym (core metadata concept)	Partial epilepsy with auditory aura	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
3763854011 - Autosomal dominant epilepsy with auditory features (en) View
3763854011	en	Synonym (core metadata concept)	Autosomal dominant epilepsy with auditory features	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3763855012 - Autosomal dominant lateral temporal lobe epilepsy (en) View
3763855012	en	Synonym (core metadata concept)	Autosomal dominant lateral 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 (11377592029) - 784377008 -> 111941005 (116680003) View
116680003 \|Is a (attribute)\|	111941005 \|Familial disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11377593023) - 784377008 -> 193000002 (116680003) View
116680003 \|Is a (attribute)\|	193000002 \|Temporal lobe epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16161274021) - 784377008 -> 1332158001 (116680003) View
116680003 \|Is a (attribute)\|	1332158001 \|Epilepsy with auditory features (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16161275022) - 784377008 -> 783739005 (116680003) View
116680003 \|Is a (attribute)\|	783739005 \|Familial temporal lobe epilepsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11377590021) - 784377008 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11377591020) - 784377008 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11574398027) - 784377008 -> 78277001 (363698007) View
363698007 \|Finding site (attribute)\|	78277001 \|Temporal lobe structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1332158001 View
1332158001	Epilepsy with auditory features (disorder)	Epilepsy with auditory features	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
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	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 (500c0ea9-c092-596b-992f-fbff8be44b5d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G40.1	TRUE	ALWAYS G40.1 \| 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 (fbc0d260-3c73-503a-87cb-fe2542eda109) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G40.0	TRUE	ALWAYS G40.0 \| 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)\|

Terminology chevron_right Concepts chevron_right 784377008

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches