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Terminology chevron_right Concepts chevron_right 1187191003

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Component

1187191003

The component that hold information about this concept.

Fully Specified Name (FSN)

Autosomal recessive spastic paraplegia type 74 (disorder)

Shortest Term

Autosomal recessive spastic paraplegia type 74

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

Autosomal recessive spastic paraplegia type 74 (disorder)

SCTID: 1187191003, Primitive, Active

1187191003|Autosomal recessive spastic paraplegia type 74 (disorder)|

en Autosomal recessive spastic paraplegia type 74
en Autosomal recessive spastic paraplegia type 74 (disorder)

Expression

1187191003 |Autosomal recessive spastic paraplegia type 74 (disorder)|
 <<< 789674008 |Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)| : 
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 68616007 |Primary atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 18234004 |Optic nerve structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 2748008 |Spinal cord structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 2667000 |Absent (qualifier value)|,
363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        { 363698007 |Finding site (attribute)| = 1264400000 |Structure of motor nervous system (body structure)| }
        { 363698007 |Finding site (attribute)| = 32153003 |Structure of left lower limb (body structure)| }
        { 363698007 |Finding site (attribute)| = 62175007 |Structure of right lower limb (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4670313019 - Autosomal recessive spastic paraplegia type 74 (en) View
4670313019	en	Synonym (core metadata concept)	Autosomal recessive spastic paraplegia type 74	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4670314013 - Autosomal recessive spastic paraplegia type 74 (disorder) (en) View
4670314013	en	Fully specified name (core metadata concept)	Autosomal recessive spastic paraplegia type 74 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16398320026) - 1187191003 -> 1264400000 (363698007) View
363698007 \|Finding site (attribute)\|	1264400000 \|Structure of motor nervous system (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277642020) - 1187191003 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14966114027) - 1187191003 -> 61685007 (363698007) View
363698007 \|Finding site (attribute)\|	61685007 \|Lower limb structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15277643026) - 1187191003 -> 32153003 (363698007) View
363698007 \|Finding site (attribute)\|	32153003 \|Structure of left lower limb (body structure)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277644021) - 1187191003 -> 62175007 (363698007) View
363698007 \|Finding site (attribute)\|	62175007 \|Structure of right lower limb (body structure)\|	7	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277645022) - 1187191003 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15277646023) - 1187191003 -> 2667000 (363713009) View
363713009 \|Has interpretation (attribute)\|	2667000 \|Absent (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14966107029) - 1187191003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14966110020) - 1187191003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14966113022) - 1187191003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14966105021) - 1187191003 -> 789674008 (116680003) View
116680003 \|Is a (attribute)\|	789674008 \|Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14966106022) - 1187191003 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14966108023) - 1187191003 -> 18234004 (363698007) View
363698007 \|Finding site (attribute)\|	18234004 \|Optic nerve structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14966109026) - 1187191003 -> 68616007 (116676008) View
116676008 \|Associated morphology (attribute)\|	68616007 \|Primary atrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14966111024) - 1187191003 -> 2748008 (363698007) View
363698007 \|Finding site (attribute)\|	2748008 \|Spinal cord structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14966112028) - 1187191003 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
789674008 View
789674008	Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)	Spoan and spoan-related disorder	900000000000074008 \|Necessary but not sufficient concept 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 (ceda7860-43d7-5be2-a740-5a1e29a9438b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G11.4	TRUE	ALWAYS G11.4 \| 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)\|

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