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Terminology chevron_right Concepts chevron_right 93244008

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Component

93244008

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital hypoplasia of basisphenoid bone (disorder)

Shortest Term

Congenital small 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 hypoplasia of basisphenoid bone (disorder)

SCTID: 93244008, Defined, Active

93244008|Congenital hypoplasia of basisphenoid bone (disorder)|

en Congenital hypoplasia of basisphenoid bone
en Congenital hypoplasia of basisphenoid bone (disorder)
en Congenital small basisphenoid bone

Expression

93244008 |Congenital hypoplasia of basisphenoid bone (disorder)|
 === 92996006 |Congenital anomaly of basisphenoid bone (disorder)| + 
1145427001 |Congenital hypoplasia of bone of cranium (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (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
154277011 - Congenital hypoplasia of basisphenoid bone (en) View
154277011	en	Synonym (core metadata concept)	Congenital hypoplasia of basisphenoid bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
836937012 - Congenital hypoplasia of basisphenoid bone (disorder) (en) View
836937012	en	Fully specified name (core metadata concept)	Congenital hypoplasia of basisphenoid bone (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
154278018 - Congenital small basisphenoid bone (en) View
154278018	en	Synonym (core metadata concept)	Congenital small basisphenoid bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16384933023) - 93244008 -> 1145427001 (116680003) View
116680003 \|Is a (attribute)\|	1145427001 \|Congenital hypoplasia of bone of cranium (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (915123029) - 93244008 -> 156145000 (363698007) View
363698007 \|Finding site (attribute)\|	156145000 \|Structure of basisphenoid bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4972403029) - 93244008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989284028) - 93244008 -> 156145000 (363698007) View
363698007 \|Finding site (attribute)\|	156145000 \|Structure of basisphenoid bone (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5002783020) - 93244008 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6092967024) - 93244008 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6092968025) - 93244008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10530981027) - 93244008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (915122023) - 93244008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2233071023) - 93244008 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3394377024) - 93244008 -> 156145000 (363698007) View
363698007 \|Finding site (attribute)\|	156145000 \|Structure of basisphenoid bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3394378025) - 93244008 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3394379022) - 93244008 -> 38146002 (116676008) View
116676008 \|Associated morphology (attribute)\|	38146002 \|Congenital hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (915121027) - 93244008 -> 38146002 (116676008) View
116676008 \|Associated morphology (attribute)\|	38146002 \|Congenital hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (915124024) - 93244008 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (301845020) - 93244008 -> 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
1145427001 View
1145427001	Congenital hypoplasia of bone of cranium (disorder)	Cranial hypoplasia	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 (2004ed93-41b8-5702-968e-a646217c01ec) 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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