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Terminology chevron_right Concepts chevron_right 38096003

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Component

38096003

The component that hold information about this concept.

Fully Specified Name (FSN)

Functional asplenia (disorder)

Shortest Term

Functional asplenia

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

Functional asplenia (disorder)

SCTID: 38096003, Primitive, Active

38096003|Functional asplenia (disorder)|

en Functional asplenia
en Functional asplenia (disorder)

Expression

38096003 |Functional asplenia (disorder)|
 <<< 707147002 |Asplenia (disorder)| : 
        { 363698007 |Finding site (attribute)| = 78961009 |Splenic structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
64686013 - Functional asplenia (en) View
64686013	en	Synonym (core metadata concept)	Functional asplenia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
770995016 - Functional asplenia (disorder) (en) View
770995016	en	Fully specified name (core metadata concept)	Functional asplenia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
64687016 - Congenital asplenia (en) View
64687016	en	Synonym (core metadata concept)	Congenital asplenia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4721950029) - 38096003 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4722189021) - 38096003 -> 51244008 (116680003) View
116680003 \|Is a (attribute)\|	51244008 \|Disorder of spleen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5980591025) - 38096003 -> 707147002 (116680003) View
116680003 \|Is a (attribute)\|	707147002 \|Asplenia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (209901022) - 38096003 -> 93030006 (116680003) View
116680003 \|Is a (attribute)\|	93030006 \|Congenital absence of spleen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (767094025) - 38096003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (767095029) - 38096003 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (767096028) - 38096003 -> 55641003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55641003 \|Infarct (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (767097021) - 38096003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2770581027) - 38096003 -> 417163006 (116680003) View
116680003 \|Is a (attribute)\|	417163006 \|Traumatic and/or non-traumatic injury (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3219270028) - 38096003 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3245838022) - 38096003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3257715024) - 38096003 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (767098027) - 38096003 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2595122024) - 38096003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1765375022) - 38096003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
707147002 View
707147002	Asplenia (disorder)	Asplenia	900000000000074008 \|Necessary but not sufficient concept 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 (2991c426-b158-5d64-9abc-1c0a2ca0d797) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q89.0	TRUE	ALWAYS Q89.0 \| MAPPED FOLLOWING WHO GUIDANCE	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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