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Terminology chevron_right Concepts chevron_right 734031008

Production

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Component

734031008

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital absence of optic chiasma (disorder)

Shortest Term

Congenital achiasma

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 absence of optic chiasma (disorder)

SCTID: 734031008, Defined, Active

734031008|Congenital absence of optic chiasma (disorder)|

en Congenital absence of optic chiasma
en Congenital absence of optic chiasma (disorder)
en Congenital achiasma

Expression

734031008 |Congenital absence of optic chiasma (disorder)|
 === 70476006 |Optic chiasm disorder (disorder)| + 
127329003 |Congenital anomaly of visual system (disorder)| + 
85641006 |Hemianencephaly (disorder)| + 
11701009 |Hemicephaly (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 727986007 |Entire optic chiasma (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
3482043013 - Congenital absence of optic chiasma (en) View
3482043013	en	Synonym (core metadata concept)	Congenital absence of optic chiasma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3482041010 - Congenital absence of optic chiasma (disorder) (en) View
3482041010	en	Fully specified name (core metadata concept)	Congenital absence of optic chiasma (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3482042015 - Congenital achiasma (en) View
3482042015	en	Synonym (core metadata concept)	Congenital achiasma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14025664024) - 734031008 -> 702628006 (116680003) View
116680003 \|Is a (attribute)\|	702628006 \|Congenital anomaly of cerebrum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16327484026) - 734031008 -> 11701009 (116680003) View
116680003 \|Is a (attribute)\|	11701009 \|Hemicephaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14025663029) - 734031008 -> 26595007 (116680003) View
116680003 \|Is a (attribute)\|	26595007 \|Congenital absence of part of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16088999028) - 734031008 -> 85641006 (116680003) View
116680003 \|Is a (attribute)\|	85641006 \|Hemianencephaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7109614022) - 734031008 -> 87290003 (116680003) View
116680003 \|Is a (attribute)\|	87290003 \|Congenital anomaly of head (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7109616024) - 734031008 -> 128124001 (116680003) View
116680003 \|Is a (attribute)\|	128124001 \|Congenital anomaly of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7109618020) - 734031008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13182727028) - 734031008 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7109617026) - 734031008 -> 702626005 (116680003) View
116680003 \|Is a (attribute)\|	702626005 \|Congenital absence (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10521802020) - 734031008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7109613027) - 734031008 -> 70476006 (116680003) View
116680003 \|Is a (attribute)\|	70476006 \|Optic chiasm disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7109615023) - 734031008 -> 127329003 (116680003) View
116680003 \|Is a (attribute)\|	127329003 \|Congenital anomaly of visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7109619028) - 734031008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7109620023) - 734031008 -> 727986007 (363698007) View
363698007 \|Finding site (attribute)\|	727986007 \|Entire optic chiasma (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

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
70476006 View
70476006	Optic chiasm disorder (disorder)	Chiasma syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
127329003 View
127329003	Congenital anomaly of visual system (disorder)	Congenital anomaly of visual system	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 (a2c2c8ba-d0c1-5592-ae27-a4dc8c5b034b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H47.4	TRUE	ALWAYS H47.4 \| 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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