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Terminology chevron_right Concepts chevron_right 93087002

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Component

93087002

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital fenestration of presphenoid bone (disorder)

Shortest Term

Congenital presphenoid hole

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 fenestration of presphenoid bone (disorder)

SCTID: 93087002, Defined, Active

93087002|Congenital fenestration of presphenoid bone (disorder)|

en Congenital fenestration of presphenoid bone
en Congenital fenestration of presphenoid bone (disorder)
en Congenital presphenoid hole

Expression

93087002 |Congenital fenestration of presphenoid bone (disorder)|
 === 93020002 |Congenital anomaly of presphenoid bone (disorder)| + 
879976004 |Lesion of bone (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 16255008 |Fenestration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 156448007 |Structure of presphenoidal bone (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
153992013 - Congenital fenestration of presphenoid bone (en) View
153992013	en	Synonym (core metadata concept)	Congenital fenestration of presphenoid bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
836746010 - Congenital fenestration of presphenoid bone (disorder) (en) View
836746010	en	Fully specified name (core metadata concept)	Congenital fenestration of presphenoid bone (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
153993015 - Congenital presphenoid hole (en) View
153993015	en	Synonym (core metadata concept)	Congenital presphenoid hole	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16413184021) - 93087002 -> 879976004 (116680003) View
116680003 \|Is a (attribute)\|	879976004 \|Lesion of bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11301184027) - 93087002 -> 36191001 (116676008) View
116676008 \|Associated morphology (attribute)\|	36191001 \|Perforation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13187147021) - 93087002 -> 16255008 (116676008) View
116676008 \|Associated morphology (attribute)\|	16255008 \|Fenestration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (914067021) - 93087002 -> 88890009 (116676008) View
116676008 \|Associated morphology (attribute)\|	88890009 \|Congenital perforation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (914065029) - 93087002 -> 156448007 (363698007) View
363698007 \|Finding site (attribute)\|	156448007 \|Structure of presphenoidal bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4972827023) - 93087002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989912025) - 93087002 -> 156448007 (363698007) View
363698007 \|Finding site (attribute)\|	156448007 \|Structure of presphenoidal bone (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5028764027) - 93087002 -> 88890009 (116676008) View
116676008 \|Associated morphology (attribute)\|	88890009 \|Congenital perforation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6092854022) - 93087002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514954027) - 93087002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (914064025) - 93087002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2233022029) - 93087002 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3363859023) - 93087002 -> 88890009 (116676008) View
116676008 \|Associated morphology (attribute)\|	88890009 \|Congenital perforation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3443541020) - 93087002 -> 156448007 (363698007) View
363698007 \|Finding site (attribute)\|	156448007 \|Structure of presphenoidal bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3466970024) - 93087002 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (914066028) - 93087002 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (301523027) - 93087002 -> 93020002 (116680003) View
116680003 \|Is a (attribute)\|	93020002 \|Congenital anomaly of presphenoid bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
879976004 View
879976004	Lesion of bone (disorder)	Lesion of bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93020002 View
93020002	Congenital anomaly of presphenoid bone (disorder)	Congenital anomaly of presphenoid bone	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 (08adaa52-f02a-53f6-aba8-54e82801ec70) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q75.8	TRUE	ALWAYS Q75.8	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)\|
ExtendedMap object (978413a9-4784-558f-9bd7-d73348f4d69c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q75.0	TRUE	ALWAYS Q75.0	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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