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Terminology chevron_right Concepts chevron_right 204044008

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Extended Map with ID “92bee5d8-a4da-5147-b53b-ebe663112dca” doesn’t exist. Perhaps it was deleted?

Component

204044008

The component that hold information about this concept.

Fully Specified Name (FSN)

Aplasia of corpus callosum (disorder)

Shortest Term

Aplasia of corpus callosum

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

Aplasia of corpus callosum (disorder)

SCTID: 204044008, Defined, Active

204044008|Aplasia of corpus callosum (disorder)|

en Aplasia of corpus callosum
en Aplasia of corpus callosum (disorder)

Expression

204044008 |Aplasia of corpus callosum (disorder)|
 === 11701009 |Hemicephaly (disorder)| + 
85641006 |Hemianencephaly (disorder)| + 
702611008 |Congenital brain aplasia (disorder)| + 
204042007 |Congenital malformation of corpus callosum (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 45486003 |Aplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 88442005 |Corpus callosum 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
312895015 - Aplasia of corpus callosum (en) View
312895015	en	Synonym (core metadata concept)	Aplasia of corpus callosum	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
589217018 - Aplasia of corpus callosum (disorder) (en) View
589217018	en	Fully specified name (core metadata concept)	Aplasia of corpus callosum (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16327477023) - 204044008 -> 11701009 (116680003) View
116680003 \|Is a (attribute)\|	11701009 \|Hemicephaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (330582028) - 204044008 -> 204042007 (116680003) View
116680003 \|Is a (attribute)\|	204042007 \|Congenital malformation of corpus callosum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619048023) - 204044008 -> 22811006 (116680003) View
116680003 \|Is a (attribute)\|	22811006 \|Leukoencephalopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12128968029) - 204044008 -> 85641006 (116680003) View
116680003 \|Is a (attribute)\|	85641006 \|Hemianencephaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12128969021) - 204044008 -> 702611008 (116680003) View
116680003 \|Is a (attribute)\|	702611008 \|Congenital brain aplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12128970022) - 204044008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12128971021) - 204044008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2700896029) - 204044008 -> 81308009 (116680003) View
116680003 \|Is a (attribute)\|	81308009 \|Disorder of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2773959026) - 204044008 -> 230764002 (116680003) View
116680003 \|Is a (attribute)\|	230764002 \|Congenital and developmental anomalies of the nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (969883021) - 204044008 -> 88442005 (363698007) View
363698007 \|Finding site (attribute)\|	88442005 \|Corpus callosum structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2743467021) - 204044008 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3374671022) - 204044008 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3442223024) - 204044008 -> 88442005 (363698007) View
363698007 \|Finding site (attribute)\|	88442005 \|Corpus callosum structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2700895025) - 204044008 -> 301766008 (116680003) View
116680003 \|Is a (attribute)\|	301766008 \|Lesion of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (969881023) - 204044008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (969886029) - 204044008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (969884026) - 204044008 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (969885025) - 204044008 -> 21483005 (363698007) View
363698007 \|Finding site (attribute)\|	21483005 \|Structure of central nervous system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (969882027) - 204044008 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
11701009 View
11701009	Hemicephaly (disorder)	Hemicephaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85641006 View
85641006	Hemianencephaly (disorder)	Hemicrania	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
702611008 View
702611008	Congenital brain aplasia (disorder)	Congenital brain aplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
204042007 View
204042007	Congenital malformation of corpus callosum (disorder)	Dysgenesis of corpus callosum	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
719947004 View
719947004	Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome (disorder)	Temtamy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
720819006 View
720819006	Curry jones syndrome (disorder)	Curry jones syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253140003 View
253140003	Partial agenesis of corpus callosum (disorder)	Partial agenesis of corpus callosum	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
5102002 View
5102002	Agenesis of corpus callosum (disorder)	Absent corpus callosum	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
80651009 View
80651009	Aicardi's syndrome (disorder)	Aicardi syndrome	900000000000074008 \|Necessary but not sufficient concept 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 (5ae4d2a4-95a8-5650-a8fc-021f0ba0482a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q04.0	TRUE	ALWAYS Q04.0	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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