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Terminology chevron_right Concepts chevron_right 766934006

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Component

766934006

The component that hold information about this concept.

Fully Specified Name (FSN)

Isolated unilateral hemispheric cerebellar hypoplasia (disorder)

Shortest Term

Isolated unilateral hemispheric cerebellar hypoplasia

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Isolated unilateral hemispheric cerebellar hypoplasia (disorder)

SCTID: 766934006, Primitive, Active

766934006|Isolated unilateral hemispheric cerebellar hypoplasia (disorder)|

en Isolated unilateral hemispheric cerebellar hypoplasia
en Isolated unilateral hemispheric cerebellar hypoplasia (disorder)

Expression

766934006 |Isolated unilateral hemispheric cerebellar hypoplasia (disorder)|
 <<< 298364001 |Finding of head region (finding)| + 
16026008 |Congenital cerebellar hypoplasia (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 6566002 |Cerebellar hemisphere structure (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
3663220015 - Isolated unilateral hemispheric cerebellar hypoplasia (en) View
3663220015	en	Synonym (core metadata concept)	Isolated unilateral hemispheric cerebellar hypoplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3663218018 - Isolated unilateral hemispheric cerebellar hypoplasia (disorder) (en) View
3663218018	en	Fully specified name (core metadata concept)	Isolated unilateral hemispheric cerebellar hypoplasia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9298917021) - 766934006 -> 372073000 (363698007) View
363698007 \|Finding site (attribute)\|	372073000 \|Cerebral hemisphere structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13917377020) - 766934006 -> 298364001 (116680003) View
116680003 \|Is a (attribute)\|	298364001 \|Finding of head region (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16293136022) - 766934006 -> 1144337000 (116680003) View
116680003 \|Is a (attribute)\|	1144337000 \|Congenital hypoplasia of cerebral hemisphere (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16332652025) - 766934006 -> 16026008 (116680003) View
116680003 \|Is a (attribute)\|	16026008 \|Congenital cerebellar hypoplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16332653024) - 766934006 -> 6566002 (363698007) View
363698007 \|Finding site (attribute)\|	6566002 \|Cerebellar hemisphere structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9298918027) - 766934006 -> 93249003 (116680003) View
116680003 \|Is a (attribute)\|	93249003 \|Congenital hypoplasia of cerebrum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10532924027) - 766934006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9298915029) - 766934006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9298916028) - 766934006 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
298364001 View
298364001	Finding of head region (finding)	Finding of head region	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
16026008 View
16026008	Congenital cerebellar hypoplasia (disorder)	Cerebellar hypoplasia	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 (f75f862e-5064-5dc9-8118-a836060569e0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q04.3	TRUE	ALWAYS Q04.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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