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Terminology chevron_right Concepts chevron_right 449682004

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Component

449682004

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital absence of part of upper limb (disorder)

Shortest Term

Congenital absence of part of upper limb

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

Congenital absence of part of upper limb (disorder)

SCTID: 449682004, Defined, Active

449682004|Congenital absence of part of upper limb (disorder)|

en Congenital absence of part of upper limb
en Congenital absence of part of upper limb (disorder)

Expression

449682004 |Congenital absence of part of upper limb (disorder)|
 === 360526007 |Congenital absence of upper limb (disorder)| + 
60220000 |Partial congenital absence of limb (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 120574008 |Upper extremity part (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2912610011 - Congenital absence of part of upper limb (en) View
2912610011	en	Synonym (core metadata concept)	Congenital absence of part of upper limb	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2912975011 - Congenital absence of part of upper limb (disorder) (en) View
2912975011	en	Fully specified name (core metadata concept)	Congenital absence of part of upper limb (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5004037024) - 449682004 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13183772026) - 449682004 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10529254023) - 449682004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4600443023) - 449682004 -> 60220000 (116680003) View
116680003 \|Is a (attribute)\|	60220000 \|Partial congenital absence of limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4600441020) - 449682004 -> 88456007 (116676008) View
116676008 \|Associated morphology (attribute)\|	88456007 \|Congenital partial absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4600444028) - 449682004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4600445027) - 449682004 -> 53120007 (363698007) View
363698007 \|Finding site (attribute)\|	53120007 \|Upper limb structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4979214028) - 449682004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5004038025) - 449682004 -> 120574008 (363698007) View
363698007 \|Finding site (attribute)\|	120574008 \|Upper extremity part (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4600442029) - 449682004 -> 360526007 (116680003) View
116680003 \|Is a (attribute)\|	360526007 \|Congenital absence of upper limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
360526007 View
360526007	Congenital absence of upper limb (disorder)	Congenital absence of upper limb	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60220000 View
60220000	Partial congenital absence of limb (disorder)	Meromelia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1145380003 View
1145380003	Aplasia of muscle of upper limb (disorder)	Aplasia of muscle of upper limb	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1145400000 View
1145400000	Aplasia of radial artery (disorder)	Aplasia of radial artery	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1145451006 View
1145451006	Aplasia of bone of upper limb (disorder)	Aplasia of bone of upper limb	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
3699000 View
3699000	Transverse deficiency of upper limb (disorder)	Transverse arrest of the arm	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
253926000 View
253926000	Phocomelia of the upper limb (disorder)	Phocomelia of upper limb	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
771261002 View
771261002	Digital extensor muscle aplasia with polyneuropathy (disorder)	Hamanishi ueba tsuji syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
449683009 View
449683009	Congenital absence of part of upper arm (disorder)	Congenital absence of part of upper arm	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
71084008 View
71084008	Congenital absence of arm and forearm (disorder)	Congenital absence of arm and forearm	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
371199008 View
371199008	Congenital absence of hand (disorder)	Acheiria	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
52022007 View
52022007	Congenital absence of ulna (disorder)	Ulnar hemimelia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
84918006 View
84918006	Congenital absence of radius (disorder)	Radial hemimelia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
91873009 View
91873009	Congenital absence of carpal bone (disorder)	Agenesis of carpal bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
91908000 View
91908000	Congenital absence of scapula (disorder)	Agenesis of scapula	900000000000073002 \|Sufficiently defined by necessary conditions 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 (da78d745-5434-5ef2-8ca4-fbf3be7d8fba) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q71.9	TRUE	ALWAYS Q71.9	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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