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Terminology chevron_right Concepts chevron_right 773396009

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Component

773396009

The component that hold information about this concept.

Fully Specified Name (FSN)

Distal arthrogryposis type 5d (disorder)

Shortest Term

Distal arthrogryposis type 5d

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

Distal arthrogryposis type 5d (disorder)

SCTID: 773396009, Primitive, Active

773396009|Distal arthrogryposis type 5d (disorder)|

en Da5d - distal arthrogryposis type 5d
en Distal arthrogryposis type 5d
en Distal arthrogryposis type 5d (disorder)
en Distal arthrogryposis type 5 without ophthalmoparesis
en Distal arthrogryposis type 5 without ophthalmoplegia

Expression

773396009 |Distal arthrogryposis type 5d (disorder)|
 <<< 28204005 |Inherited arthrogryposis (disorder)| + 
205402004 |Arthrogryposis multiplex congenita (disorder)| + 
24269006 |Distal arthrogryposis syndrome (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (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
3723379017 - DA5D - distal arthrogryposis type 5D (en) View
3723379017	en	Synonym (core metadata concept)	DA5D - distal arthrogryposis type 5D	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3723376012 - Distal arthrogryposis type 5D (en) View
3723376012	en	Synonym (core metadata concept)	Distal arthrogryposis type 5D	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3723375011 - Distal arthrogryposis type 5D (disorder) (en) View
3723375011	en	Fully specified name (core metadata concept)	Distal arthrogryposis type 5D (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3723377015 - Distal arthrogryposis type 5 without ophthalmoparesis (en) View
3723377015	en	Synonym (core metadata concept)	Distal arthrogryposis type 5 without ophthalmoparesis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3723378013 - Distal arthrogryposis type 5 without ophthalmoplegia (en) View
3723378013	en	Synonym (core metadata concept)	Distal arthrogryposis type 5 without ophthalmoplegia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16198014023) - 773396009 -> 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 (16198015024) - 773396009 -> 57048009 (116676008) View
116676008 \|Associated morphology (attribute)\|	57048009 \|Contracture (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15507984027) - 773396009 -> 28204005 (116680003) View
116680003 \|Is a (attribute)\|	28204005 \|Inherited arthrogryposis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15508048023) - 773396009 -> 205402004 (116680003) View
116680003 \|Is a (attribute)\|	205402004 \|Arthrogryposis multiplex congenita (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10599336026) - 773396009 -> 39352004 (363698007) View
363698007 \|Finding site (attribute)\|	39352004 \|Joint structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11512116023) - 773396009 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11512117025) - 773396009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11512118024) - 773396009 -> 364564000 (363714003) View
363714003 \|Interprets (attribute)\|	364564000 \|Range of joint movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11512119027) - 773396009 -> 785818007 (363698007) View
363698007 \|Finding site (attribute)\|	785818007 \|Structure of joint region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10599332029) - 773396009 -> 57048009 (116676008) View
116676008 \|Associated morphology (attribute)\|	57048009 \|Contracture (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10599333023) - 773396009 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10599334028) - 773396009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10599335027) - 773396009 -> 24269006 (116680003) View
116680003 \|Is a (attribute)\|	24269006 \|Distal arthrogryposis syndrome (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
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
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

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (949f61c4-8b21-5335-9f97-8115dd6db248) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q68.8	TRUE	ALWAYS Q68.8 \| 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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