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Terminology chevron_right Concepts chevron_right 80378000

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Component

80378000

The component that hold information about this concept.

Fully Specified Name (FSN)

Neonatal hepatosplenomegaly (disorder)

Shortest Term

Gan lách to sơ sinh

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

Neonatal hepatosplenomegaly (disorder)

SCTID: 80378000, Defined, Active

80378000|Neonatal hepatosplenomegaly (disorder)|

vi Gan lách to sơ sinh
en Neonatal hepatosplenomegaly
en Neonatal hepatosplenomegaly (disorder)

Expression

80378000 |Neonatal hepatosplenomegaly (disorder)|
 === 42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| + 
36760000 |Hepatosplenomegaly (disorder)| + 
414028007 |Disorder of hematopoietic system in newborn (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 181268008 |Entire liver (body structure)|,
246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 181279003 |Entire spleen (body structure)|,
246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
452521000003117 - gan lách to sơ sinh (vi) View
452521000003117	vi	Synonym (core metadata concept)	gan lách to sơ sinh	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
133378017 - Neonatal hepatosplenomegaly (en) View
133378017	en	Synonym (core metadata concept)	Neonatal hepatosplenomegaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
821531011 - Neonatal hepatosplenomegaly (disorder) (en) View
821531011	en	Fully specified name (core metadata concept)	Neonatal hepatosplenomegaly (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9657003025) - 80378000 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3583263024) - 80378000 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3615420025) - 80378000 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4662824025) - 80378000 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4662825029) - 80378000 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4662826028) - 80378000 -> 181268008 (363698007) View
363698007 \|Finding site (attribute)\|	181268008 \|Entire liver (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4662827021) - 80378000 -> 181279003 (363698007) View
363698007 \|Finding site (attribute)\|	181279003 \|Entire spleen (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13633739022) - 80378000 -> 181268008 (363698007) View
363698007 \|Finding site (attribute)\|	181268008 \|Entire liver (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13633740024) - 80378000 -> 181279003 (363698007) View
363698007 \|Finding site (attribute)\|	181279003 \|Entire spleen (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13633741023) - 80378000 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (874738028) - 80378000 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3609248025) - 80378000 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3615421026) - 80378000 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (874740022) - 80378000 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (874741021) - 80378000 -> 56246009 (116676008) View
116676008 \|Associated morphology (attribute)\|	56246009 \|Hypertrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3310274028) - 80378000 -> 56246009 (116676008) View
116676008 \|Associated morphology (attribute)\|	56246009 \|Hypertrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3445183023) - 80378000 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (874739020) - 80378000 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2697291026) - 80378000 -> 276548008 (116680003) View
116680003 \|Is a (attribute)\|	276548008 \|Perinatal disorders of liver and/or biliary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (278666028) - 80378000 -> 363219007 (116680003) View
116680003 \|Is a (attribute)\|	363219007 \|Neonatal gastrointestinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2602076028) - 80378000 -> 122865005 (363698007) View
363698007 \|Finding site (attribute)\|	122865005 \|Gastrointestinal tract structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2697292022) - 80378000 -> 414028007 (116680003) View
116680003 \|Is a (attribute)\|	414028007 \|Disorder of hematopoietic system in newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (278665029) - 80378000 -> 36760000 (116680003) View
116680003 \|Is a (attribute)\|	36760000 \|Hepatosplenomegaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
36760000 View
36760000	Hepatosplenomegaly (disorder)	Gan lách to	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
414028007 View
414028007	Disorder of hematopoietic system in newborn (disorder)	Neonatal disorder of hematopoietic 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 (3b95c700-bbb9-51f7-ab9a-9e700efb1e8e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	R16.2	TRUE	ALWAYS R16.2	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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