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Terminology chevron_right Concepts chevron_right 271018002

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Component

271018002

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital absence of tendon (disorder)

Shortest Term

Absent tendon

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 tendon (disorder)

SCTID: 271018002, Defined, Active

271018002|Congenital absence of tendon (disorder)|

en Absent tendon
en Congenital absence of tendon
en Congenital absence of tendon (disorder)

Expression

271018002 |Congenital absence of tendon (disorder)|
 === 47880003 |Congenital absence of muscle and/or tendon (disorder)| + 
68172002 |Disorder of tendon (disorder)| + 
363039000 |Congenital connective tissue disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 13024002 |Tendon structure (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
405555010 - Absent tendon (en) View
405555010	en	Synonym (core metadata concept)	Absent tendon	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
405554014 - Congenital absence of tendon (en) View
405554014	en	Synonym (core metadata concept)	Congenital absence of tendon	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
663402017 - Congenital absence of tendon (disorder) (en) View
663402017	en	Fully specified name (core metadata concept)	Congenital absence of tendon (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (596122022) - 271018002 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13180522029) - 271018002 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3449478028) - 271018002 -> 13024002 (363698007) View
363698007 \|Finding site (attribute)\|	13024002 \|Tendon structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4978953020) - 271018002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000289029) - 271018002 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000290022) - 271018002 -> 13024002 (363698007) View
363698007 \|Finding site (attribute)\|	13024002 \|Tendon structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6129399025) - 271018002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10518033029) - 271018002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (596120025) - 271018002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3373500021) - 271018002 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4790392029) - 271018002 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4790393023) - 271018002 -> 73573004 (116680003) View
116680003 \|Is a (attribute)\|	73573004 \|Congenital anomaly of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5051603020) - 271018002 -> 47880003 (116680003) View
116680003 \|Is a (attribute)\|	47880003 \|Congenital absence of muscle and/or tendon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2755075029) - 271018002 -> 38776003 (116680003) View
116680003 \|Is a (attribute)\|	38776003 \|Congenital absence of skeletal muscle (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1738585026) - 271018002 -> 13024002 (363698007) View
363698007 \|Finding site (attribute)\|	13024002 \|Tendon structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (89925025) - 271018002 -> 47880003 (116680003) View
116680003 \|Is a (attribute)\|	47880003 \|Congenital absence of muscle and/or tendon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2755073020) - 271018002 -> 363039000 (116680003) View
116680003 \|Is a (attribute)\|	363039000 \|Congenital connective tissue disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2755074025) - 271018002 -> 68172002 (116680003) View
116680003 \|Is a (attribute)\|	68172002 \|Disorder of tendon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (596121026) - 271018002 -> 79984008 (363698007) View
363698007 \|Finding site (attribute)\|	79984008 \|Skeletal muscle system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (596123028) - 271018002 -> 256667004 (363698007) View
363698007 \|Finding site (attribute)\|	256667004 \|Entire tendon (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
47880003 View
47880003	Congenital absence of muscle and/or tendon (disorder)	Congenital absence of muscle and tendon	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363039000 View
363039000	Congenital connective tissue disorder (disorder)	Congenital connective tissue disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
68172002 View
68172002	Disorder of tendon (disorder)	Tendinopathy	900000000000073002 \|Sufficiently defined by necessary conditions 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 (8e71e9a6-a746-5e47-a78c-a7f335622301) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q79.8	TRUE	ALWAYS Q79.8	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)\|

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