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Terminology chevron_right Concepts chevron_right 1208615009

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Component

1208615009

The component that hold information about this concept.

Fully Specified Name (FSN)

Neurogenic scapuloperoneal syndrome kaeser type (disorder)

Shortest Term

Kaeser syndrome

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

Neurogenic scapuloperoneal syndrome kaeser type (disorder)

SCTID: 1208615009, Primitive, Active

1208615009|Neurogenic scapuloperoneal syndrome kaeser type (disorder)|

en Kaeser syndrome
en Neurogenic scapuloperoneal syndrome kaeser type
en Neurogenic scapuloperoneal syndrome kaeser type (disorder)
en Stark kaeser syndrome

Expression

1208615009 |Neurogenic scapuloperoneal syndrome kaeser type (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
257277002 |Combined disorder of muscle and peripheral nerve (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
49793008 |Hereditary motor neuron disease (disorder)| + 
1119438000 |Atrophy of muscle of shoulder (disorder)| + 
1142324004 |Atrophy of peroneal muscle (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 102288007 |Structure of skeletal muscle of shoulder (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 25442002 |Peroneal 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
4965394014 - Kaeser syndrome (en) View
4965394014	en	Synonym (core metadata concept)	Kaeser syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4965395010 - Neurogenic scapuloperoneal syndrome Kaeser type (en) View
4965395010	en	Synonym (core metadata concept)	Neurogenic scapuloperoneal syndrome Kaeser type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
4965393015 - Neurogenic scapuloperoneal syndrome Kaeser type (disorder) (en) View
4965393015	en	Fully specified name (core metadata concept)	Neurogenic scapuloperoneal syndrome Kaeser type (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
4965392013 - Stark Kaeser syndrome (en) View
4965392013	en	Synonym (core metadata concept)	Stark Kaeser syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16298909023) - 1208615009 -> 1119440005 (116680003) View
116680003 \|Is a (attribute)\|	1119440005 \|Atrophy of muscle of lower leg (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16299005024) - 1208615009 -> 1142324004 (116680003) View
116680003 \|Is a (attribute)\|	1142324004 \|Atrophy of peroneal muscle (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098375027) - 1208615009 -> 118944007 (116680003) View
116680003 \|Is a (attribute)\|	118944007 \|Disorder of shoulder region (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15098376026) - 1208615009 -> 128137003 (116680003) View
116680003 \|Is a (attribute)\|	128137003 \|Disorder of lower leg (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15098378025) - 1208615009 -> 280136002 (116680003) View
116680003 \|Is a (attribute)\|	280136002 \|Disorder of soft tissue of lower limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15098381024) - 1208615009 -> 88092000 (116680003) View
116680003 \|Is a (attribute)\|	88092000 \|Muscle atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16298908026) - 1208615009 -> 1119438000 (116680003) View
116680003 \|Is a (attribute)\|	1119438000 \|Atrophy of muscle of shoulder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098374028) - 1208615009 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098377024) - 1208615009 -> 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 (15098379022) - 1208615009 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098380020) - 1208615009 -> 49793008 (116680003) View
116680003 \|Is a (attribute)\|	49793008 \|Hereditary motor neuron disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098382028) - 1208615009 -> 3058005 (363698007) View
363698007 \|Finding site (attribute)\|	3058005 \|Peripheral nervous system structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098383022) - 1208615009 -> 102288007 (363698007) View
363698007 \|Finding site (attribute)\|	102288007 \|Structure of skeletal muscle of shoulder (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098384027) - 1208615009 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098385026) - 1208615009 -> 25442002 (363698007) View
363698007 \|Finding site (attribute)\|	25442002 \|Peroneal muscle structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15098386025) - 1208615009 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1142324004 View
1142324004	Atrophy of peroneal muscle (disorder)	Atrophy of peroneal muscle	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1119438000 View
1119438000	Atrophy of muscle of shoulder (disorder)	Atrophy of muscle of shoulder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
49793008 View
49793008	Hereditary motor neuron disease (disorder)	Familial motor neuron disease	900000000000074008 \|Necessary but not sufficient concept 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
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

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 (e86e14bc-ec09-5c97-8be6-08f1f207cf99) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G12.1	TRUE	ALWAYS G12.1 \| 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)\|

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