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Terminology chevron_right Concepts chevron_right 92946005

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Component

92946005

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital abnormal shape of spleen (disorder)

Shortest Term

Congenital misshapen spleen

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 abnormal shape of spleen (disorder)

SCTID: 92946005, Defined, Active

92946005|Congenital abnormal shape of spleen (disorder)|

en Congenital abnormal shape of spleen
en Congenital abnormal shape of spleen (disorder)
en Congenital misshapen spleen

Expression

92946005 |Congenital abnormal shape of spleen (disorder)|
 === 57497006 |Congenital anomaly of spleen (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 399984000 |Abnormal shape (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 181279003 |Entire spleen (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
153707015 - Congenital abnormal shape of spleen (en) View
153707015	en	Synonym (core metadata concept)	Congenital abnormal shape of spleen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
836576017 - Congenital abnormal shape of spleen (disorder) (en) View
836576017	en	Fully specified name (core metadata concept)	Congenital abnormal shape of spleen (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
153708013 - Congenital misshapen spleen (en) View
153708013	en	Synonym (core metadata concept)	Congenital misshapen spleen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (913040022) - 92946005 -> 43948000 (116676008) View
116676008 \|Associated morphology (attribute)\|	43948000 \|Congenital abnormal shape (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11322524025) - 92946005 -> 399984000 (116676008) View
116676008 \|Associated morphology (attribute)\|	399984000 \|Abnormal shape (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4978340028) - 92946005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5014745026) - 92946005 -> 43948000 (116676008) View
116676008 \|Associated morphology (attribute)\|	43948000 \|Congenital abnormal shape (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5014746025) - 92946005 -> 181279003 (363698007) View
363698007 \|Finding site (attribute)\|	181279003 \|Entire spleen (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6092693026) - 92946005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6092694021) - 92946005 -> 181279003 (363698007) View
363698007 \|Finding site (attribute)\|	181279003 \|Entire spleen (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10528716027) - 92946005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (913038028) - 92946005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2232962024) - 92946005 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2552819020) - 92946005 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3391694028) - 92946005 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3391695027) - 92946005 -> 43948000 (116676008) View
116676008 \|Associated morphology (attribute)\|	43948000 \|Congenital abnormal shape (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3443513021) - 92946005 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3453856026) - 92946005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (913039020) - 92946005 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (913041021) - 92946005 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2604254027) - 92946005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1783461021) - 92946005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (301261025) - 92946005 -> 57497006 (116680003) View
116680003 \|Is a (attribute)\|	57497006 \|Congenital anomaly of spleen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
57497006 View
57497006	Congenital anomaly of spleen (disorder)	Anomalies of spleen	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 (9163cc1e-47b7-5ae0-b9d9-6ff4dc23a958) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q89.0	TRUE	ALWAYS Q89.0	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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