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Terminology chevron_right Concepts chevron_right 763691008

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Component

763691008

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial isolated clinodactyly of finger (disorder)

Shortest Term

Familial isolated clinodactyly of finger

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

Familial isolated clinodactyly of finger (disorder)

SCTID: 763691008, Primitive, Active

763691008|Familial isolated clinodactyly of finger (disorder)|

en Familial isolated clinodactyly of finger
en Familial isolated clinodactyly of finger (disorder)

Expression

763691008 |Familial isolated clinodactyly of finger (disorder)|
 <<< 1003620005 |Congenital clinodactyly of finger (disorder)| + 
782964007 |Genetic disease (disorder)| + 
111941005 |Familial disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 38392006 |Congenital abnormal curvature (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 7569003 |Finger 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
3643298012 - Familial isolated clinodactyly of finger (en) View
3643298012	en	Synonym (core metadata concept)	Familial isolated clinodactyly of finger	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3643297019 - Familial isolated clinodactyly of finger (disorder) (en) View
3643297019	en	Fully specified name (core metadata concept)	Familial isolated clinodactyly of finger (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9132131028) - 763691008 -> 17268007 (116680003) View
116680003 \|Is a (attribute)\|	17268007 \|Congenital clinodactyly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9132135021) - 763691008 -> 12406000 (363698007) View
363698007 \|Finding site (attribute)\|	12406000 \|Little finger structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13184247020) - 763691008 -> 1003620005 (116680003) View
116680003 \|Is a (attribute)\|	1003620005 \|Congenital clinodactyly of finger (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13184248026) - 763691008 -> 782964007 (116680003) View
116680003 \|Is a (attribute)\|	782964007 \|Genetic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13184249023) - 763691008 -> 7569003 (363698007) View
363698007 \|Finding site (attribute)\|	7569003 \|Finger structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532412028) - 763691008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132132024) - 763691008 -> 111941005 (116680003) View
116680003 \|Is a (attribute)\|	111941005 \|Familial disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132133025) - 763691008 -> 38392006 (116676008) View
116676008 \|Associated morphology (attribute)\|	38392006 \|Congenital abnormal curvature (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132134020) - 763691008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1003620005 View
1003620005	Congenital clinodactyly of finger (disorder)	Congenital crooked finger	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
782964007 View
782964007	Genetic disease (disorder)	Genetic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
111941005 View
111941005	Familial disease (disorder)	Familial disease	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 (c33cdc05-d278-5a98-ae52-43826af7e83e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q68.1	TRUE	ALWAYS Q68.1	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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