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Terminology chevron_right Concepts chevron_right 111246005

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Extended Map with ID “9daf6aeb-e6fe-5b60-8b3a-cbed8e090974” doesn’t exist. Perhaps it was deleted?

Component

111246005

The component that hold information about this concept.

Fully Specified Name (FSN)

Arthrogryposis (disorder)

Shortest Term

Arthrogryposis

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

Arthrogryposis (disorder)

SCTID: 111246005, Defined, Active

111246005|Arthrogryposis (disorder)|

en Arthrogryposis
en Arthrogryposis (disorder)

Expression

111246005 |Arthrogryposis (disorder)|
 === 202264009 |Contracture of multiple joints (disorder)| + 
276655000 |Congenital deformity (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)| }
        { 363713009 |Has interpretation (attribute)| = 1250004 |Decreased (qualifier value)|,
363714003 |Interprets (attribute)| = 364564000 |Range of joint movement (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 57048009 |Contracture (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 773190007 |Joint structure of multiple body sites (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3769051013 - AMC-Arthrogryposis multiplex congenita (en) View
3769051013	en	Synonym (core metadata concept)	AMC-Arthrogryposis multiplex congenita	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
3769034018 - Arthrogryposis multiplex congenita (en) View
3769034018	en	Synonym (core metadata concept)	Arthrogryposis multiplex congenita	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
3769038015 - Congenital multiple arthrogryposis (en) View
3769038015	en	Synonym (core metadata concept)	Congenital multiple arthrogryposis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
2161656011 - Guerin-Stern syndrome (en) View
2161656011	en	Synonym (core metadata concept)	Guerin-Stern syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
178465011 - Arthrogryposis (en) View
178465011	en	Synonym (core metadata concept)	Arthrogryposis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
629629010 - Arthrogryposis (disorder) (en) View
629629010	en	Fully specified name (core metadata concept)	Arthrogryposis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16198059026) - 111246005 -> 773190007 (363698007) View
363698007 \|Finding site (attribute)\|	773190007 \|Joint structure of multiple body sites (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16198060020) - 111246005 -> 57048009 (116676008) View
116676008 \|Associated morphology (attribute)\|	57048009 \|Contracture (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (57424023) - 111246005 -> 7890003 (116680003) View
116680003 \|Is a (attribute)\|	7890003 \|Contracture of joint (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (536880028) - 111246005 -> 57048009 (116676008) View
116676008 \|Associated morphology (attribute)\|	57048009 \|Contracture (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6034233023) - 111246005 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6034234028) - 111246005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6034235027) - 111246005 -> 57048009 (116676008) View
116676008 \|Associated morphology (attribute)\|	57048009 \|Contracture (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6034236026) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6094927024) - 111246005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11439939025) - 111246005 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11439940028) - 111246005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11439941029) - 111246005 -> 202264009 (116680003) View
116680003 \|Is a (attribute)\|	202264009 \|Contracture of multiple joints (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11439942020) - 111246005 -> 785818007 (363698007) View
363698007 \|Finding site (attribute)\|	785818007 \|Structure of joint region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11439943026) - 111246005 -> 276655000 (116680003) View
116680003 \|Is a (attribute)\|	276655000 \|Congenital deformity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11439944021) - 111246005 -> 364564000 (363714003) View
363714003 \|Interprets (attribute)\|	364564000 \|Range of joint movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (57425024) - 111246005 -> 95463009 (116680003) View
116680003 \|Is a (attribute)\|	95463009 \|Congenital anomaly of joint (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3093823022) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4978078022) - 111246005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4978079025) - 111246005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4988226024) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (536879026) - 111246005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2576068020) - 111246005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3093824027) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2979620029) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2979621025) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2914736024) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2914737026) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2821837023) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2821838029) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2674880025) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2674881026) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (536878023) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2525214027) - 111246005 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1657770025) - 111246005 -> 64162006 (116680003) View
116680003 \|Is a (attribute)\|	64162006 \|Multiple malformation syndrome with unusual brain and/or neuromuscular findings (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1731853028) - 111246005 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2254625025) - 111246005 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1731854023) - 111246005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
202264009 View
202264009	Contracture of multiple joints (disorder)	Co cứng nhiều khớp	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
276655000 View
276655000	Congenital deformity (disorder)	Congenital deformity	900000000000073002 \|Sufficiently defined by necessary conditions definition status (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
1264194006 View
1264194006	Congenital amyoplasia (disorder)	Amyoplasia congenita	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
370473000 View
370473000	Congenital arthrogryposis caused by teratogen (disorder)	Congenital arthrogryposis due to teratogen	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
24269006 View
24269006	Distal arthrogryposis syndrome (disorder)	Distal arthrogryposis	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 (32d3a889-c161-5197-8727-716e834b24c7) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q68.8	TRUE	ALWAYS Q68.8	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 (38d9879f-1f4b-59ce-a532-239ecc36a0e0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q68.8	IFA 370473000 \| Congenital arthrogryposis due to teratogen (disorder) \|	IF CONGENITAL ARTHROGRYPOSIS DUE TO TERATOGEN CHOOSE Q68.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE	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 (3cb498dc-66dc-5f5d-8a66-b4f5d56eda59) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q68.8	OTHERWISE TRUE	ALWAYS Q68.8	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 (59c27e9a-94a1-5017-a9b0-04603951ed86) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q74.3	IFA 77016009 \| Amyoplasia congenita disruptive sequence (disorder) \|	IF AMYOPLASIA CONGENITA DISRUPTIVE SEQUENCE CHOOSE Q74.3 \| 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)\|

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