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Terminology chevron_right Concepts chevron_right 93236008

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Component

93236008

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital hypoplasia of alisphenoid bone (disorder)

Shortest Term

Congenital small alisphenoid 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 alisphenoid bone (disorder)

SCTID: 93236008, Defined, Active

93236008|Congenital hypoplasia of alisphenoid bone (disorder)|

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

Expression

93236008 |Congenital hypoplasia of alisphenoid bone (disorder)|
 === 92992008 |Congenital anomaly of alisphenoid bone (disorder)| + 
1145427001 |Congenital hypoplasia of bone of cranium (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 37724000 |Structure of greater wing of sphenoid 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
154261010 - Congenital hypoplasia of alisphenoid bone (en) View
154261010	en	Synonym (core metadata concept)	Congenital hypoplasia of alisphenoid bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
836927019 - Congenital hypoplasia of alisphenoid bone (disorder) (en) View
836927019	en	Fully specified name (core metadata concept)	Congenital hypoplasia of alisphenoid bone (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
154262015 - Congenital small alisphenoid bone (en) View
154262015	en	Synonym (core metadata concept)	Congenital small alisphenoid bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13054160025) - 93236008 -> 254026007 (116680003) View
116680003 \|Is a (attribute)\|	254026007 \|Craniofacial microsomia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16299217025) - 93236008 -> 1145427001 (116680003) View
116680003 \|Is a (attribute)\|	1145427001 \|Congenital hypoplasia of bone of cranium (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (915080026) - 93236008 -> 37724000 (363698007) View
363698007 \|Finding site (attribute)\|	37724000 \|Structure of greater wing of sphenoid bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4972958023) - 93236008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4990130027) - 93236008 -> 37724000 (363698007) View
363698007 \|Finding site (attribute)\|	37724000 \|Structure of greater wing of sphenoid bone (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5002843023) - 93236008 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6092953026) - 93236008 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6092954021) - 93236008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10521325027) - 93236008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (915078021) - 93236008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3286368028) - 93236008 -> 431768007 (116680003) View
116680003 \|Is a (attribute)\|	431768007 \|Congenital malformation of sphenoid wing (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3537248023) - 93236008 -> 37724000 (363698007) View
363698007 \|Finding site (attribute)\|	37724000 \|Structure of greater wing of sphenoid bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3537249026) - 93236008 -> 38146002 (116676008) View
116676008 \|Associated morphology (attribute)\|	38146002 \|Congenital hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (915079029) - 93236008 -> 38146002 (116676008) View
116676008 \|Associated morphology (attribute)\|	38146002 \|Congenital hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2233064029) - 93236008 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2698890020) - 93236008 -> 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 (3197386024) - 93236008 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3212163020) - 93236008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (301831025) - 93236008 -> 92992008 (116680003) View
116680003 \|Is a (attribute)\|	92992008 \|Congenital anomaly of alisphenoid 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
92992008 View
92992008	Congenital anomaly of alisphenoid bone (disorder)	Congenital anomaly of alisphenoid 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 (4f9a28ef-6837-593b-9a1b-eb981173c26b) 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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