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Terminology chevron_right Concepts chevron_right 715316005

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Component

715316005

The component that hold information about this concept.

Fully Specified Name (FSN)

Neurogenic arthrogryposis multiplex congenita (disorder)

Shortest Term

Neurogenic arthrogryposis multiplex congenita

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 arthrogryposis multiplex congenita (disorder)

SCTID: 715316005, Primitive, Active

715316005|Neurogenic arthrogryposis multiplex congenita (disorder)|

en Neurogenic arthrogryposis multiplex congenita
en Neurogenic arthrogryposis multiplex congenita (disorder)

Expression

715316005 |Neurogenic arthrogryposis multiplex congenita (disorder)|
 <<< 51891008 |Polyarthropathy associated with another disorder (disorder)| + 
205402004 |Arthrogryposis multiplex congenita (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
28204005 |Inherited arthrogryposis (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 57048009 |Contracture (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 785818007 |Structure of joint region (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 57048009 |Contracture (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 773190007 |Joint structure of multiple body sites (body structure)| }
        { 42752001 |Due to (attribute)| = 74035001 |Denervation atrophy of muscle (disorder)| }
        { 363713009 |Has interpretation (attribute)| = 1250004 |Decreased (qualifier value)|,
363714003 |Interprets (attribute)| = 364564000 |Range of joint movement (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3302195017 - Neurogenic arthrogryposis multiplex congenita (en) View
3302195017	en	Synonym (core metadata concept)	Neurogenic arthrogryposis multiplex congenita	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3302194018 - Neurogenic arthrogryposis multiplex congenita (disorder) (en) View
3302194018	en	Fully specified name (core metadata concept)	Neurogenic arthrogryposis multiplex congenita (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6594652025) - 715316005 -> 57048009 (116676008) View
116676008 \|Associated morphology (attribute)\|	57048009 \|Contracture (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16198045022) - 715316005 -> 51891008 (116680003) View
116680003 \|Is a (attribute)\|	51891008 \|Polyarthropathy associated with another disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16198046023) - 715316005 -> 773190007 (363698007) View
363698007 \|Finding site (attribute)\|	773190007 \|Joint structure of multiple body sites (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11512086027) - 715316005 -> 364564000 (363714003) View
363714003 \|Interprets (attribute)\|	364564000 \|Range of joint movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11512088026) - 715316005 -> 2667000 (363713009) View
363713009 \|Has interpretation (attribute)\|	2667000 \|Absent (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11512089023) - 715316005 -> 298224003 (116680003) View
116680003 \|Is a (attribute)\|	298224003 \|Joint movement absent (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15507923020) - 715316005 -> 205402004 (116680003) View
116680003 \|Is a (attribute)\|	205402004 \|Arthrogryposis multiplex congenita (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594647024) - 715316005 -> 74035001 (42752001) View
42752001 \|Due to (attribute)\|	74035001 \|Denervation atrophy of muscle (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594648025) - 715316005 -> 35524003 (116680003) View
116680003 \|Is a (attribute)\|	35524003 \|Arthropathy associated with another disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6594650022) - 715316005 -> 111246005 (116680003) View
116680003 \|Is a (attribute)\|	111246005 \|Arthrogryposis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6594651021) - 715316005 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6594653024) - 715316005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6594654029) - 715316005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11512081021) - 715316005 -> 57048009 (116676008) View
116676008 \|Associated morphology (attribute)\|	57048009 \|Contracture (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11512083024) - 715316005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11512084029) - 715316005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11512087020) - 715316005 -> 785818007 (363698007) View
363698007 \|Finding site (attribute)\|	785818007 \|Structure of joint region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11512090025) - 715316005 -> 28204005 (116680003) View
116680003 \|Is a (attribute)\|	28204005 \|Inherited arthrogryposis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11570214023) - 715316005 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11570215024) - 715316005 -> 364564000 (363714003) View
363714003 \|Interprets (attribute)\|	364564000 \|Range of joint movement (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594649022) - 715316005 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
205402004 View
205402004	Arthrogryposis multiplex congenita (disorder)	Multiple congenital arthrogryposis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
51891008 View
51891008	Polyarthropathy associated with another disorder (disorder)	Polyarthropathy associated with another disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
28204005 View
28204005	Inherited arthrogryposis (disorder)	Inherited arthrogryposis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
720513002 View
720513002	Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder)	Arc (arthrogryposis, renal dysfunction, cholestasis) 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 (081bb118-fd39-560d-8b98-166c4c8dbe4c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q74.3	TRUE	ALWAYS Q74.3 \| 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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