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Terminology chevron_right Concepts chevron_right 57497006

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Component

57497006

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of spleen (disorder)

Shortest Term

Anomalies of 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 anomaly of spleen (disorder)

SCTID: 57497006, Defined, Active

57497006|Congenital anomaly of spleen (disorder)|

en Anomalies of spleen
en Congenital abnormality of spleen
en Congenital anomaly of spleen
en Congenital anomaly of spleen (disorder)
en Congenital malformation of spleen

Expression

57497006 |Congenital anomaly of spleen (disorder)|
 === 363024001 |Congenital anomaly of abdomen (disorder)| + 
51244008 |Disorder of spleen (disorder)| + 
40888008 |Congenital anomaly of the hematopoietic system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 78961009 |Splenic 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
497906012 - Anomalies of spleen (en) View
497906012	en	Synonym (core metadata concept)	Anomalies of spleen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
497907015 - Congenital abnormality of spleen (en) View
497907015	en	Synonym (core metadata concept)	Congenital abnormality of spleen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
95610012 - Congenital anomaly of spleen (en) View
95610012	en	Synonym (core metadata concept)	Congenital anomaly of spleen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
796125013 - Congenital anomaly of spleen (disorder) (en) View
796125013	en	Fully specified name (core metadata concept)	Congenital anomaly of spleen (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
497905011 - Congenital malformation of spleen (en) View
497905011	en	Synonym (core metadata concept)	Congenital malformation of spleen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
95611011 - Congenital anomaly of spleen, NOS (en) View
95611011	en	Synonym (core metadata concept)	Congenital anomaly of spleen, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (816604025) - 57497006 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4977344024) - 57497006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4977345020) - 57497006 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4977346021) - 57497006 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6080250029) - 57497006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10527977021) - 57497006 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10527978027) - 57497006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (816603020) - 57497006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3374650028) - 57497006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3374651029) - 57497006 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2694168029) - 57497006 -> 363026004 (116680003) View
116680003 \|Is a (attribute)\|	363026004 \|Congenital anomaly of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1771714023) - 57497006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2548826022) - 57497006 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2694167023) - 57497006 -> 363024001 (116680003) View
116680003 \|Is a (attribute)\|	363024001 \|Congenital anomaly of abdomen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (241634022) - 57497006 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (816605029) - 57497006 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (241632021) - 57497006 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (241631025) - 57497006 -> 40888008 (116680003) View
116680003 \|Is a (attribute)\|	40888008 \|Congenital anomaly of the hematopoietic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (241633027) - 57497006 -> 51244008 (116680003) View
116680003 \|Is a (attribute)\|	51244008 \|Disorder of spleen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363024001 View
363024001	Congenital anomaly of abdomen (disorder)	Congenital anomaly of abdomen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
51244008 View
51244008	Disorder of spleen (disorder)	Spleen disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
40888008 View
40888008	Congenital anomaly of the hematopoietic system (disorder)	Congenital anomaly of the hematopoietic system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
62042001 View
62042001	Splenogonadal fusion (disorder)	Splenogonadal fusion	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
717156002 View
717156002	Biliary atresia with splenic malformation syndrome (disorder)	Basm syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
42780004 View
42780004	Congenital lobulation of spleen (disorder)	Lobulation of spleen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
702624008 View
702624008	Aplasia of spleen (disorder)	Splenic aplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
234501002 View
234501002	Epidermoid cyst of spleen (disorder)	Epidermoid cyst of spleen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
10362008 View
10362008	Accessory spleen (disorder)	Splenunculi	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
36752001 View
36752001	Congenital splenomegaly (disorder)	Congenital splenomegaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
65146007 View
65146007	Ectopic spleen (disorder)	Ectopic spleen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
92946005 View
92946005	Congenital abnormal shape of spleen (disorder)	Congenital misshapen spleen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93030006 View
93030006	Congenital absence of spleen (disorder)	Splenic aplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93049005 View
93049005	Congenital cyst of spleen (disorder)	Serous cyst of spleen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93292008 View
93292008	Congenital hypoplasia of spleen (disorder)	Congenital microsplenia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93351001 View
93351001	Congenital malposition of spleen (disorder)	Congenital malpositioned spleen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
205736006 View
205736006	Mis-shapen spleen (disorder)	Mis-shapen spleen	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 (000f269e-9c6f-5b7a-9f54-cc8e495825a0) 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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