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Terminology chevron_right Concepts chevron_right 789674008

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)

Shortest Term

Spoan and spoan-related disorder

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

Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)

SCTID: 789674008, Primitive, Active

789674008|Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)|

en Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder
en Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)
en Spoan and spoan-related disorder

Expression

789674008 |Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)|
 <<< 1370930009 |Cranial nerve palsy (disorder)| + 
26360005 |Hereditary optic atrophy (disorder)| + 
230261006 |Complicated hereditary spastic paraplegia (disorder)| + 
1187279003 |Autosomal recessive hereditary spastic paraplegia (disorder)| + 
106152006 |Second cranial nerve finding (finding)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 2748008 |Spinal cord structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 68616007 |Primary atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 18234004 |Optic nerve structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 62175007 |Structure of right lower limb (body structure)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 2667000 |Absent (qualifier value)|,
363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        { 363698007 |Finding site (attribute)| = 32153003 |Structure of left lower limb (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
3791514016 - Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (en) View
3791514016	en	Synonym (core metadata concept)	Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3791515015 - Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder) (en) View
3791515015	en	Fully specified name (core metadata concept)	Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3791513010 - SPOAN and SPOAN-related disorder (en) View
3791513010	en	Synonym (core metadata concept)	SPOAN and SPOAN-related disorder	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16398154024) - 789674008 -> 1264400000 (363698007) View
363698007 \|Finding site (attribute)\|	1264400000 \|Structure of motor nervous system (body structure)\|	7	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16351011026) - 789674008 -> 784289008 (116680003) View
116680003 \|Is a (attribute)\|	784289008 \|Nerve palsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16406212024) - 789674008 -> 1370930009 (116680003) View
116680003 \|Is a (attribute)\|	1370930009 \|Cranial nerve palsy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277097025) - 789674008 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	7	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103025023) - 789674008 -> 61685007 (363698007) View
363698007 \|Finding site (attribute)\|	61685007 \|Lower limb structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15277096023) - 789674008 -> 106152006 (116680003) View
116680003 \|Is a (attribute)\|	106152006 \|Second cranial nerve finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277098024) - 789674008 -> 62175007 (363698007) View
363698007 \|Finding site (attribute)\|	62175007 \|Structure of right lower limb (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277099027) - 789674008 -> 32153003 (363698007) View
363698007 \|Finding site (attribute)\|	32153003 \|Structure of left lower limb (body structure)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277100024) - 789674008 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277101023) - 789674008 -> 2667000 (363713009) View
363713009 \|Has interpretation (attribute)\|	2667000 \|Absent (qualifier value)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103014025) - 789674008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103017021) - 789674008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103018027) - 789674008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103020029) - 789674008 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103024022) - 789674008 -> 698292000 (116680003) View
116680003 \|Is a (attribute)\|	698292000 \|Chronic paraplegia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12103027026) - 789674008 -> 722990003 (116680003) View
116680003 \|Is a (attribute)\|	722990003 \|Congenital atrophy of optic nerve (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14969604020) - 789674008 -> 1187279003 (116680003) View
116680003 \|Is a (attribute)\|	1187279003 \|Autosomal recessive hereditary spastic paraplegia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103015029) - 789674008 -> 2748008 (363698007) View
363698007 \|Finding site (attribute)\|	2748008 \|Spinal cord structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103016028) - 789674008 -> 18234004 (363698007) View
363698007 \|Finding site (attribute)\|	18234004 \|Optic nerve structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103019024) - 789674008 -> 68616007 (116676008) View
116676008 \|Associated morphology (attribute)\|	68616007 \|Primary atrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103021025) - 789674008 -> 26360005 (116680003) View
116680003 \|Is a (attribute)\|	26360005 \|Hereditary optic atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103022021) - 789674008 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103023027) - 789674008 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12103026024) - 789674008 -> 230261006 (116680003) View
116680003 \|Is a (attribute)\|	230261006 \|Complicated hereditary spastic paraplegia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1370930009 View
1370930009	Cranial nerve palsy (disorder)	Cranial nerve palsy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1187279003 View
1187279003	Autosomal recessive hereditary spastic paraplegia (disorder)	Autosomal recessive hereditary spastic paraplegia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
106152006 View
106152006	Second cranial nerve finding (finding)	Optic nerve finding	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
26360005 View
26360005	Hereditary optic atrophy (disorder)	Hereditary optic atrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
230261006 View
230261006	Complicated hereditary spastic paraplegia (disorder)	Complicated hereditary spastic paraplegia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1187191003 View
1187191003	Autosomal recessive spastic paraplegia type 74 (disorder)	Autosomal recessive spastic paraplegia type 74	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
723825006 View
723825006	Autosomal recessive spastic paraplegia type 55 (disorder)	Autosomal recessive spastic paraplegia type 55	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
723826007 View
723826007	Autosomal recessive spastic paraplegia type 57 (disorder)	Autosomal recessive spastic paraplegia type 57	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
725139005 View
725139005	Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)	Spastic paraplegia, optic atrophy, neuropathy 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 (0c96774c-8b4b-518b-82fd-112dcdf96054) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G60.0	TRUE	ALWAYS G60.0 \| 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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