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Terminology chevron_right Concepts chevron_right 1237365009

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Component

1237365009

The component that hold information about this concept.

Fully Specified Name (FSN)

Aprosencephaly/atelencephaly spectrum (disorder)

Shortest Term

Aprosencephaly/atelencephaly spectrum

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

Aprosencephaly/atelencephaly spectrum (disorder)

SCTID: 1237365009, Primitive, Active

1237365009|Aprosencephaly/atelencephaly spectrum (disorder)|

en Aprosencephaly/atelencephaly spectrum
en Aprosencephaly/atelencephaly spectrum (disorder)

Expression

1237365009 |Aprosencephaly/atelencephaly spectrum (disorder)|
 <<< 253128003 |Abnormality of neurogenesis (disorder)| + 
702628006 |Congenital anomaly of cerebrum (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 83678007 |Cerebral 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
5098002015 - Aprosencephaly/atelencephaly spectrum (en) View
5098002015	en	Synonym (core metadata concept)	Aprosencephaly/atelencephaly spectrum	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5098003013 - Aprosencephaly/atelencephaly spectrum (disorder) (en) View
5098003013	en	Fully specified name (core metadata concept)	Aprosencephaly/atelencephaly spectrum (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15295361020) - 1237365009 -> 609521009 (116680003) View
116680003 \|Is a (attribute)\|	609521009 \|Disorder of embryonic structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15295364028) - 1237365009 -> 81861006 (363698007) View
363698007 \|Finding site (attribute)\|	81861006 \|Prosencephalon structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15835720026) - 1237365009 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15295360021) - 1237365009 -> 253128003 (116680003) View
116680003 \|Is a (attribute)\|	253128003 \|Abnormality of neurogenesis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15295362029) - 1237365009 -> 702628006 (116680003) View
116680003 \|Is a (attribute)\|	702628006 \|Congenital anomaly of cerebrum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15295363023) - 1237365009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15295365027) - 1237365009 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15295366026) - 1237365009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
702628006 View
702628006	Congenital anomaly of cerebrum (disorder)	Congenital anomaly of cerebrum	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
253128003 View
253128003	Abnormality of neurogenesis (disorder)	Abnormality of neurogenesis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
277921008 View
277921008	Atelencephaly (disorder)	Atelencephaly	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
277922001 View
277922001	Aprosencephaly (disorder)	Aprosencephaly	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 (15b1200d-8ef9-52eb-98e0-0af3463f2faf) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q04.8	TRUE	ALWAYS Q04.8 \| 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)\|
ExtendedMap object (43c31c46-abe7-5a70-a89f-c4e172f36032) 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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