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Terminology chevron_right Concepts chevron_right 783257005

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Component

783257005

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial recurrent peripheral facial palsy (disorder)

Shortest Term

Familial recurrent bell palsy

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

Familial recurrent peripheral facial palsy (disorder)

SCTID: 783257005, Primitive, Active

783257005|Familial recurrent peripheral facial palsy (disorder)|

en Familial recurrent bell palsy
en Familial recurrent peripheral facial palsy
en Familial recurrent peripheral facial palsy (disorder)

Expression

783257005 |Familial recurrent peripheral facial palsy (disorder)|
 <<< 193093009 |Bell's palsy (disorder)| + 
111941005 |Familial disease (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 2667000 |Absent (qualifier value)|,
363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        { 363698007 |Finding site (attribute)| = 56052001 |Facial nerve structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 1264400000 |Structure of motor nervous system (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3758312018 - Familial recurrent Bell palsy (en) View
3758312018	en	Synonym (core metadata concept)	Familial recurrent Bell palsy	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
3758310014 - Familial recurrent peripheral facial palsy (en) View
3758310014	en	Synonym (core metadata concept)	Familial recurrent peripheral facial palsy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3758311013 - Familial recurrent peripheral facial palsy (disorder) (en) View
3758311013	en	Fully specified name (core metadata concept)	Familial recurrent peripheral facial palsy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16398291022) - 783257005 -> 1264400000 (363698007) View
363698007 \|Finding site (attribute)\|	1264400000 \|Structure of motor nervous system (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11284776024) - 783257005 -> 249893002 (363714003) View
363714003 \|Interprets (attribute)\|	249893002 \|Gross movement of body and limbs (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094638021) - 783257005 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15246250021) - 783257005 -> 364729007 (116680003) View
116680003 \|Is a (attribute)\|	364729007 \|Finding of gross movement of body and limbs (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15246251020) - 783257005 -> 784289008 (116680003) View
116680003 \|Is a (attribute)\|	784289008 \|Nerve palsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16351035020) - 783257005 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11284774022) - 783257005 -> 2667000 (363713009) View
363713009 \|Has interpretation (attribute)\|	2667000 \|Absent (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11284775023) - 783257005 -> 193093009 (116680003) View
116680003 \|Is a (attribute)\|	193093009 \|Bell's palsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11284777026) - 783257005 -> 111941005 (116680003) View
116680003 \|Is a (attribute)\|	111941005 \|Familial disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11571510024) - 783257005 -> 56052001 (363698007) View
363698007 \|Finding site (attribute)\|	56052001 \|Facial nerve structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
111941005 View
111941005	Familial disease (disorder)	Familial disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
193093009 View
193093009	Bell's palsy (disorder)	Liệt	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 (a1c0bcc1-7b77-53fc-a84a-5f4b0a0e1b85) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G51.0	TRUE	ALWAYS G51.0	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)\|

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