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Terminology chevron_right Concepts chevron_right 771187008

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Language with ID “3054eb5d-c513-5b81-8d0b-7cce28154587” doesn’t exist. Perhaps it was deleted?

Component

771187008

The component that hold information about this concept.

Fully Specified Name (FSN)

Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)

Shortest Term

Cacp syndrome

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

Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)

SCTID: 771187008, Primitive, Active

771187008|Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)|

en Arthropathy camptodactyly syndrome
en Cacp (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome
en Cacp syndrome
en Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome
en Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)
en Jacobs syndrome
en Pericarditis, arthropathy, camptodactyly syndrome

Expression

771187008 |Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)|
 <<< 36186002 |Polyarthropathy (disorder)| + 
302942008 |Fixed flexion deformity finger (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
896876006 |Structural abnormality of interphalangeal joint of hand (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 788600005 |Fixed flexion deformity (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 371232006 |Proximal interphalangeal joint of finger structure (body structure)| }
        { 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
3704820010 - Arthropathy camptodactyly syndrome (en) View
3704820010	en	Synonym (core metadata concept)	Arthropathy camptodactyly syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3704824018 - CACP (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome (en) View
3704824018	en	Synonym (core metadata concept)	CACP (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3704825017 - CACP syndrome (en) View
3704825017	en	Synonym (core metadata concept)	CACP syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3704819016 - Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (en) View
3704819016	en	Synonym (core metadata concept)	Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3704822019 - Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) (en) View
3704822019	en	Fully specified name (core metadata concept)	Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3704823012 - Jacobs syndrome (en) View
3704823012	en	Synonym (core metadata concept)	Jacobs syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3704821014 - Pericarditis, arthropathy, camptodactyly syndrome (en) View
3704821014	en	Synonym (core metadata concept)	Pericarditis, arthropathy, camptodactyly syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16379287029) - 771187008 -> 896876006 (116680003) View
116680003 \|Is a (attribute)\|	896876006 \|Structural abnormality of interphalangeal joint of hand (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648306024) - 771187008 -> 203554005 (116680003) View
116680003 \|Is a (attribute)\|	203554005 \|Flexion deformity of finger (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9648309028) - 771187008 -> 88565003 (116676008) View
116676008 \|Associated morphology (attribute)\|	88565003 \|Flexion deformity (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094952020) - 771187008 -> 788600005 (116676008) View
116676008 \|Associated morphology (attribute)\|	788600005 \|Fixed flexion deformity (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094953026) - 771187008 -> 302942008 (116680003) View
116680003 \|Is a (attribute)\|	302942008 \|Fixed flexion deformity finger (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10590873029) - 771187008 -> 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 (9648307026) - 771187008 -> 371232006 (363698007) View
363698007 \|Finding site (attribute)\|	371232006 \|Proximal interphalangeal joint of finger structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648308020) - 771187008 -> 36186002 (116680003) View
116680003 \|Is a (attribute)\|	36186002 \|Polyarthropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648310022) - 771187008 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648311021) - 771187008 -> 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
896876006 View
896876006	Structural abnormality of interphalangeal joint of hand (disorder)	Abnormal phalangeal joint of hand morphology	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
302942008 View
302942008	Fixed flexion deformity finger (disorder)	Fixed flexion deformity finger	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
36186002 View
36186002	Polyarthropathy (disorder)	Polyarthrosis	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
363212003 View
363212003	Hereditary disorder of musculoskeletal system (disorder)	Hereditary disorder of musculoskeletal system	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 (4e0efc65-d838-582f-9947-c4b7b3a42578) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	M12.89	TRUE	ALWAYS M12.89 \| 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)\|
ExtendedMap object (65f4d0b3-225a-5887-804e-32c85c96178d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.5	TRUE	ALWAYS Q87.5 \| 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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