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Terminology chevron_right Concepts chevron_right 92996006

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Component

92996006

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of basisphenoid bone (disorder)

Shortest Term

Congenital anomaly 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

Congenital anomaly of basisphenoid bone (disorder)

SCTID: 92996006, Defined, Active

92996006|Congenital anomaly of basisphenoid bone (disorder)|

en Congenital anomaly of basisphenoid bone
en Congenital anomaly of basisphenoid bone (disorder)

Expression

92996006 |Congenital anomaly of basisphenoid bone (disorder)|
 === 51655004 |Congenital anomaly of skull (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (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
153810019 - Congenital anomaly of basisphenoid bone (en) View
153810019	en	Synonym (core metadata concept)	Congenital anomaly of basisphenoid bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
836636017 - Congenital anomaly of basisphenoid bone (disorder) (en) View
836636017	en	Fully specified name (core metadata concept)	Congenital anomaly of basisphenoid bone (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
153811015 - Congenital anomaly of basisphenoid bone, NOS (en) View
153811015	en	Synonym (core metadata concept)	Congenital anomaly of basisphenoid bone, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4995809024) - 92996006 -> 93003001 (116680003) View
116680003 \|Is a (attribute)\|	93003001 \|Congenital anomaly of fetal head bones (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16384932029) - 92996006 -> 51655004 (116680003) View
116680003 \|Is a (attribute)\|	51655004 \|Congenital anomaly of skull (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (913422025) - 92996006 -> 156145000 (363698007) View
363698007 \|Finding site (attribute)\|	156145000 \|Structure of basisphenoid bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4971862026) - 92996006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4971863020) - 92996006 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4988372021) - 92996006 -> 156145000 (363698007) View
363698007 \|Finding site (attribute)\|	156145000 \|Structure of basisphenoid bone (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6092743023) - 92996006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10519239027) - 92996006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10519240025) - 92996006 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (913421021) - 92996006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (913423024) - 92996006 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2698799025) - 92996006 -> 268239009 (116680003) View
116680003 \|Is a (attribute)\|	268239009 \|Congenital abnormality of skull and face bones (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3085393024) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3085394029) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4733155021) - 92996006 -> 609520005 (116680003) View
116680003 \|Is a (attribute)\|	609520005 \|Disorder of fetal structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4733156022) - 92996006 -> 609521009 (116680003) View
116680003 \|Is a (attribute)\|	609521009 \|Disorder of embryonic structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2965090026) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2965091027) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2899861022) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2899862026) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2806618024) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2806619027) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2657569026) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2657570025) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1783478028) - 92996006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2552829029) - 92996006 -> 93003001 (116680003) View
116680003 \|Is a (attribute)\|	93003001 \|Congenital anomaly of fetal head bones (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2049065020) - 92996006 -> 268239009 (116680003) View
116680003 \|Is a (attribute)\|	268239009 \|Congenital abnormality of skull and face bones (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (301358029) - 92996006 -> 93003001 (116680003) View
116680003 \|Is a (attribute)\|	93003001 \|Congenital anomaly of fetal head bones (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
51655004 View
51655004	Congenital anomaly of skull (disorder)	Dị tật bẩm sinh của hộp sọ	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
93569009 View
93569009	Incomplete ossification of basisphenoid bone (disorder)	Reduced ossification of basisphenoid bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93036000 View
93036000	Congenital fenestration of basisphenoid bone (disorder)	Congenital basisphenoid hole	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93244008 View
93244008	Congenital hypoplasia of basisphenoid bone (disorder)	Congenital small basisphenoid bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93625006 View
93625006	Lack of ossification of basisphenoid bone (disorder)	Unossified basisphenoid bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
91871006 View
91871006	Congenital absence of basisphenoid bone (disorder)	Agenesis of basisphenoid bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
92841001 View
92841001	Congenital abnormal fusion of basisphenoid bone (disorder)	Congenital fused basisphenoid bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
92896007 View
92896007	Congenital abnormal shape of basisphenoid bone (disorder)	Congenital misshapen basisphenoid bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (d394a9e3-9d5a-5c66-b9c5-19dcc69b2c42) 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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