dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 257277002

Production

add

Component

257277002

The component that hold information about this concept.

Fully Specified Name (FSN)

Combined disorder of muscle and peripheral nerve (disorder)

Shortest Term

Myoneural disorder

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Combined disorder of muscle and peripheral nerve (disorder)

SCTID: 257277002, Defined, Active

257277002|Combined disorder of muscle and peripheral nerve (disorder)|

en Myoneural disorder
en Neuromuscular disorder
en Combined disorder of muscle and peripheral nerve
en Combined disorder of muscle and peripheral nerve (disorder)

Expression

257277002 |Combined disorder of muscle and peripheral nerve (disorder)|
 === 42658009 |Disorder of the peripheral nervous system (disorder)| + 
75047002 |Disorder of skeletal muscle (disorder)| : 
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 3058005 |Peripheral nervous system structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
383065014 - Myoneural disorders (en) View
383065014	en	Synonym (core metadata concept)	Myoneural disorders	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
383066010 - Myoneural disorder (en) View
383066010	en	Synonym (core metadata concept)	Myoneural disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3078548014 - Neuromuscular disorder (en) View
3078548014	en	Synonym (core metadata concept)	Neuromuscular disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2669851011 - Combined disorder of muscle AND peripheral nerve (en) View
2669851011	en	Synonym (core metadata concept)	Combined disorder of muscle AND peripheral nerve	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
648550012 - Combined disorder of muscle AND peripheral nerve (disorder) (en) View
648550012	en	Fully specified name (core metadata concept)	Combined disorder of muscle AND peripheral nerve (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (585543020) - 257277002 -> 3058005 (363698007) View
363698007 \|Finding site (attribute)\|	3058005 \|Peripheral nervous system structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1737158026) - 257277002 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1659567020) - 257277002 -> 75047002 (116680003) View
116680003 \|Is a (attribute)\|	75047002 \|Disorder of skeletal muscle (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (78361028) - 257277002 -> 42658009 (116680003) View
116680003 \|Is a (attribute)\|	42658009 \|Disorder of the peripheral nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
42658009 View
42658009	Disorder of the peripheral nervous system (disorder)	Neuropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
75047002 View
75047002	Disorder of skeletal muscle (disorder)	Disorder of muscle	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1137386008 View
1137386008	Generalized hypotonia due to neuromuscular junction defect (disorder)	Generalised hypotonia due to neuromuscular junction defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1340172003 View
1340172003	Chloride voltage-gated channel 6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome (disorder)	Clcn6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
65242001 View
65242001	Drug-induced myasthenia (disorder)	Drug-induced myasthenia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1222704008 View
1222704008	Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder)	Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1208615009 View
1208615009	Neurogenic scapuloperoneal syndrome kaeser type (disorder)	Kaeser syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1179294000 View
1179294000	Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome (disorder)	Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
91637004 View
91637004	Myasthenia gravis (disorder)	Bệnh nhược cơ	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
782752005 View
782752005	Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)	Peripheral neuropathy, myopathy, hoarseness, deafness syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
787172004 View
787172004	Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder)	Childhood-onset autosomal recessive myopathy with external ophthalmoplegia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
771261002 View
771261002	Digital extensor muscle aplasia with polyneuropathy (disorder)	Hamanishi ueba tsuji syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
774153002 View
774153002	Periodic paralysis with transient compartment-like syndrome (disorder)	Periodic paralysis with transient compartment-like syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
774154008 View
774154008	Periodic paralysis with later-onset distal motor neuropathy (disorder)	Periodic paralysis with later-onset distal motor neuropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
763352005 View
763352005	Familial dyskinesia and facial myokymia (disorder)	Familial dyskinesia and facial myokymia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
763688008 View
763688008	Deafness, encephaloneuropathy, obesity, valvulopathy syndrome (disorder)	Deafness, encephaloneuropathy, obesity, valvulopathy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
723157009 View
723157009	Spastic diplegia of upper limbs (disorder)	Spastic diplegia of upper limbs	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
717266001 View
717266001	Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome (disorder)	Sando (sensory ataxic neuropathy dysarthria ophthalmoparesis) syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
423753005 View
423753005	Reflex blepharospasm (disorder)	Reflex blepharospasm	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363222009 View
363222009	Neonatal neuromuscular disorder (disorder)	Neonatal neuromuscular disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
5127009 View
5127009	Jaw-winking syndrome (disorder)	Jaw winking	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
13753008 View
13753008	Hemifacial spasm (disorder)	Co thắt nửa mặt	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
26609002 View
26609002	Neuralgic amyotrophy (disorder)	Neuralgic amyotrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
29145002 View
29145002	Schwartz-jampel syndrome (disorder)	Burton syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
43152001 View
43152001	Central core disease (disorder)	Central core disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
56989000 View
56989000	Eaton-lambert syndrome (disorder)	Myasthenic syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
58756001 View
58756001	Huntington's chorea (disorder)	Huntington chorea	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
63135006 View
63135006	Amyotonia congenita (disorder)	Amyotonia congenita	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
87842000 View
87842000	Generalized neuromuscular exhaustion syndrome (disorder)	Generalised neuromuscular exhaustion syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230675008 View
230675008	Slow channel syndrome (disorder)	Slow channel syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230687001 View
230687001	Myopathy in myasthenia gravis (disorder)	Myasthenic myopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237984008 View
237984008	Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder)	Narp syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
277190002 View
277190002	Pelagic paralysis (disorder)	Pelagic paralysis	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 (1d780fc9-fa7e-5c45-8b80-91b971f5c200) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G70.9	OTHERWISE TRUE	ALWAYS G70.9	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 (3270d3f2-c46a-598d-96d5-0ac82dd89d60) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G60.0	IFA 50548001 \| Charcot-Marie-Tooth disease (disorder) \|	IF CHARCOT-MARIE-TOOTH DISEASE CHOOSE G60.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (40a7dbe7-5906-5821-a407-b84c9a58bd27) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G54.5	IFA 26609002 \| Neuralgic amyotrophy (disorder) \|	IF NEURALGIC AMYOTROPHY CHOOSE G54.5 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (764e1763-c6f7-5e34-9d43-97e723e265d2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P94.0	IFA 363222009 \| Neonatal neuromuscular disorder (disorder) \|	IF NEONATAL NEUROMUSCULAR DISORDER CHOOSE P94.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (786447ad-07af-534e-940b-1124f7f2b304) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P94.2	IFA 205294008 \| Neonatal hypotonia (disorder) \|	IF NEONATAL HYPOTONIA CHOOSE P94.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (786a6884-dfc6-51b4-a5c3-a1ec3503248c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G70.9	TRUE	ALWAYS G70.9	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 (9fdbc9b0-a74f-559d-a228-8ef242c40cda) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	F34.1	IFA 87842000 \| Generalized neuromuscular exhaustion syndrome (disorder) \|	IF GENERALIZED NEUROMUSCULAR EXHAUSTION SYNDROME CHOOSE F34.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (1d780fc9-fa7e-5c45-8b80-91b971f5c200) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G70.9	OTHERWISE TRUE	ALWAYS G70.9	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 (3270d3f2-c46a-598d-96d5-0ac82dd89d60) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G60.0	IFA 50548001 \| Charcot-Marie-Tooth disease (disorder) \|	IF CHARCOT-MARIE-TOOTH DISEASE CHOOSE G60.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (40a7dbe7-5906-5821-a407-b84c9a58bd27) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G54.5	IFA 26609002 \| Neuralgic amyotrophy (disorder) \|	IF NEURALGIC AMYOTROPHY CHOOSE G54.5 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (764e1763-c6f7-5e34-9d43-97e723e265d2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P94.0	IFA 363222009 \| Neonatal neuromuscular disorder (disorder) \|	IF NEONATAL NEUROMUSCULAR DISORDER CHOOSE P94.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (786447ad-07af-534e-940b-1124f7f2b304) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P94.2	IFA 205294008 \| Neonatal hypotonia (disorder) \|	IF NEONATAL HYPOTONIA CHOOSE P94.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (786a6884-dfc6-51b4-a5c3-a1ec3503248c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G70.9	TRUE	ALWAYS G70.9	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 (9fdbc9b0-a74f-559d-a228-8ef242c40cda) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	F34.1	IFA 87842000 \| Generalized neuromuscular exhaustion syndrome (disorder) \|	IF GENERALIZED NEUROMUSCULAR EXHAUSTION SYNDROME CHOOSE F34.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Terminology chevron_right Concepts chevron_right 257277002

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches