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Terminology chevron_right Concepts chevron_right 93569009

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Component

93569009

The component that hold information about this concept.

Fully Specified Name (FSN)

Incomplete ossification of basisphenoid bone (disorder)

Shortest Term

Reduced ossification of basisphenoid bone

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

Incomplete ossification of basisphenoid bone (disorder)

SCTID: 93569009, Defined, Active

93569009|Incomplete ossification of basisphenoid bone (disorder)|

en Incomplete ossification of basisphenoid bone
en Incomplete ossification of basisphenoid bone (disorder)
en Reduced ossification of basisphenoid bone

Expression

93569009 |Incomplete ossification of basisphenoid bone (disorder)|
 === 92996006 |Congenital anomaly of basisphenoid bone (disorder)| + 
773586004 |Incomplete ossification of skull (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 773197005 |Incomplete ossification of bone (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 156145000 |Structure of basisphenoid 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
154904013 - Incomplete ossification of basisphenoid bone (en) View
154904013	en	Synonym (core metadata concept)	Incomplete ossification of basisphenoid bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
837329016 - Incomplete ossification of basisphenoid bone (disorder) (en) View
837329016	en	Fully specified name (core metadata concept)	Incomplete ossification of basisphenoid bone (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
154905014 - Reduced ossification of basisphenoid bone (en) View
154905014	en	Synonym (core metadata concept)	Reduced ossification of basisphenoid bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9287163027) - 93569009 -> 327877008 (116680003) View
116680003 \|Is a (attribute)\|	327877008 \|Incomplete ossification (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16384934028) - 93569009 -> 773586004 (116680003) View
116680003 \|Is a (attribute)\|	773586004 \|Incomplete ossification of skull (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (917146026) - 93569009 -> 156145000 (363698007) View
363698007 \|Finding site (attribute)\|	156145000 \|Structure of basisphenoid bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1686468023) - 93569009 -> 253980008 (116680003) View
116680003 \|Is a (attribute)\|	253980008 \|Defect of skull ossification (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4972571025) - 93569009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4972572021) - 93569009 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4979695020) - 93569009 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989554021) - 93569009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989555022) - 93569009 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4998937026) - 93569009 -> 156145000 (363698007) View
363698007 \|Finding site (attribute)\|	156145000 \|Structure of basisphenoid bone (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10529567022) - 93569009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10529568028) - 93569009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607574027) - 93569009 -> 773197005 (116676008) View
116676008 \|Associated morphology (attribute)\|	773197005 \|Incomplete ossification of bone (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1783884022) - 93569009 -> 327877008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	327877008 \|Incomplete ossification (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5029613028) - 93569009 -> 72928007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	72928007 \|Functional bone disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (917148025) - 93569009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3294718021) - 93569009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3294719029) - 93569009 -> 156145000 (363698007) View
363698007 \|Finding site (attribute)\|	156145000 \|Structure of basisphenoid bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3294720024) - 93569009 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (917147024) - 93569009 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1783885023) - 93569009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (917145027) - 93569009 -> 328891000 (116676008) View
116676008 \|Associated morphology (attribute)\|	328891000 \|Reduced ossification (finding)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (302454029) - 93569009 -> 92996006 (116680003) View
116680003 \|Is a (attribute)\|	92996006 \|Congenital anomaly of basisphenoid bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
773586004 View
773586004	Incomplete ossification of skull (disorder)	Incomplete ossification of skull	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
92996006 View
92996006	Congenital anomaly of basisphenoid bone (disorder)	Congenital anomaly of basisphenoid 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 (442b9383-03e0-5176-9947-483a8c25f1a9) 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)\|

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