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Terminology chevron_right Concepts chevron_right 763352005

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Component

763352005

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial dyskinesia and facial myokymia (disorder)

Shortest Term

Familial dyskinesia and facial myokymia

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 dyskinesia and facial myokymia (disorder)

SCTID: 763352005, Primitive, Active

763352005|Familial dyskinesia and facial myokymia (disorder)|

en Familial dyskinesia and facial myokymia
en Familial dyskinesia and facial myokymia (disorder)
en Fdfm - familial dyskinesia and facial myokymia

Expression

763352005 |Familial dyskinesia and facial myokymia (disorder)|
 <<< 1070000 |Facial myokymia (finding)| + 
9748009 |Dyskinesia (finding)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
60342002 |Movement disorder (disorder)| + 
106157000 |Seventh cranial nerve finding (finding)| + 
257277002 |Combined disorder of muscle and peripheral nerve (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
422426003 |Facial nerve disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 56052001 |Facial nerve structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        { 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
3638662013 - Familial dyskinesia and facial myokymia (en) View
3638662013	en	Synonym (core metadata concept)	Familial dyskinesia and facial myokymia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3638661018 - Familial dyskinesia and facial myokymia (disorder) (en) View
3638661018	en	Fully specified name (core metadata concept)	Familial dyskinesia and facial myokymia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3638663015 - FDFM - familial dyskinesia and facial myokymia (en) View
3638663015	en	Synonym (core metadata concept)	FDFM - familial dyskinesia and facial myokymia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16398116024) - 763352005 -> 1264400000 (363698007) View
363698007 \|Finding site (attribute)\|	1264400000 \|Structure of motor nervous system (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094998021) - 763352005 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16350683026) - 763352005 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091996021) - 763352005 -> 56052001 (363698007) View
363698007 \|Finding site (attribute)\|	56052001 \|Facial nerve structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091997028) - 763352005 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091987021) - 763352005 -> 1070000 (116680003) View
116680003 \|Is a (attribute)\|	1070000 \|Facial myokymia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091988027) - 763352005 -> 9748009 (116680003) View
116680003 \|Is a (attribute)\|	9748009 \|Dyskinesia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091989024) - 763352005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091990026) - 763352005 -> 60342002 (116680003) View
116680003 \|Is a (attribute)\|	60342002 \|Movement disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091991027) - 763352005 -> 106157000 (116680003) View
116680003 \|Is a (attribute)\|	106157000 \|Seventh cranial nerve finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091992023) - 763352005 -> 257277002 (116680003) View
116680003 \|Is a (attribute)\|	257277002 \|Combined disorder of muscle and peripheral nerve (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091993029) - 763352005 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091994024) - 763352005 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9091995020) - 763352005 -> 422426003 (116680003) View
116680003 \|Is a (attribute)\|	422426003 \|Facial nerve disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
60342002 View
60342002	Movement disorder (disorder)	Rối loạn vận động	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
422426003 View
422426003	Facial nerve disorder (disorder)	Facial neuropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
106157000 View
106157000	Seventh cranial nerve finding (finding)	Facial nerve finding	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
257277002 View
257277002	Combined disorder of muscle and peripheral nerve (disorder)	Myoneural disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1070000 View
1070000	Facial myokymia (finding)	Facial myokymia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
9748009 View
9748009	Dyskinesia (finding)	Dyskinesia	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
363212003 View
363212003	Hereditary disorder of musculoskeletal system (disorder)	Hereditary disorder of musculoskeletal system	900000000000073002 \|Sufficiently defined by necessary conditions 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 (22a80699-66d8-5c32-9ad6-01fda75ef14b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G51.4	TRUE	ALWAYS G51.4 \| 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 (a59a4c2f-cddf-5fa6-926c-2e8793949fd0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G24.8	TRUE	ALWAYS G24.8	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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