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Terminology chevron_right Concepts chevron_right 305719002

Production

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Component

305719002

The component that hold information about this concept.

Fully Specified Name (FSN)

Neuromyotonia (disorder)

Shortest Term

Neuromyotonia

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

Neuromyotonia (disorder)

SCTID: 305719002, Primitive, Active

305719002|Neuromyotonia (disorder)|

en Continuous muscle fiber activity
en Continuous muscle fibre activity
en Neuromyotonia
en Neuromyotonia (disorder)

Expression

305719002 |Neuromyotonia (disorder)|
 <<< 37340000 |Motor neuron disease (disorder)| + 
302226006 |Peripheral nerve disease (disorder)| : 
        { 363698007 |Finding site (attribute)| = 84782009 |Peripheral nerve structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
448236012 - Continuous muscle fiber activity (en) View
448236012	en	Synonym (core metadata concept)	Continuous muscle fiber activity	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
448239017 - Continuous muscle fibre activity (en) View
448239017	en	Synonym (core metadata concept)	Continuous muscle fibre activity	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
448235011 - Neuromyotonia (en) View
448235011	en	Synonym (core metadata concept)	Neuromyotonia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
702048016 - Neuromyotonia (disorder) (en) View
702048016	en	Fully specified name (core metadata concept)	Neuromyotonia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
448237015 - Gamstorp-Wohlfart syndrome (en) View
448237015	en	Synonym (core metadata concept)	Gamstorp-Wohlfart syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
448238013 - Gamstorp disease (en) View
448238013	en	Synonym (core metadata concept)	Gamstorp disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6230666020) - 305719002 -> 84782009 (363698007) View
363698007 \|Finding site (attribute)\|	84782009 \|Peripheral nerve structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (132421027) - 305719002 -> 230651008 (116680003) View
116680003 \|Is a (attribute)\|	230651008 \|Disorders of spinal neurones manifest by hyperactivity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (666546026) - 305719002 -> 2748008 (363698007) View
363698007 \|Finding site (attribute)\|	2748008 \|Spinal cord structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4737266022) - 305719002 -> 609610009 (363698007) View
363698007 \|Finding site (attribute)\|	609610009 \|Structure of nerve root and/or plexus (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6230664023) - 305719002 -> 37340000 (116680003) View
116680003 \|Is a (attribute)\|	37340000 \|Motor neuron disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6230665024) - 305719002 -> 302226006 (116680003) View
116680003 \|Is a (attribute)\|	302226006 \|Peripheral nerve disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
302226006 View
302226006	Peripheral nerve disease (disorder)	Peripheral neuropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
37340000 View
37340000	Motor neuron disease (disorder)	Motor neuron disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
711406009 View
711406009	Autosomal recessive axonal neuropathy with neuromyotonia (disorder)	Gamstorp-wohlfart syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (4a50e527-b62c-5ff4-9c60-7dd7c8909c83) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G71.1	TRUE	ALWAYS G71.1 \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE	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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