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Terminology chevron_right Concepts chevron_right 36752001

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Component

36752001

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital splenomegaly (disorder)

Shortest Term

Congenital splenomegaly

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 splenomegaly (disorder)

SCTID: 36752001, Defined, Active

36752001|Congenital splenomegaly (disorder)|

en Congenital splenomegaly
en Congenital splenomegaly (disorder)

Expression

36752001 |Congenital splenomegaly (disorder)|
 === 16294009 |Splenomegaly (disorder)| + 
57497006 |Congenital anomaly of spleen (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (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
61305016 - Congenital splenomegaly (en) View
61305016	en	Synonym (core metadata concept)	Congenital splenomegaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
768540016 - Congenital splenomegaly (disorder) (en) View
768540016	en	Fully specified name (core metadata concept)	Congenital splenomegaly (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6074726029) - 36752001 -> 441880008 (116676008) View
116676008 \|Associated morphology (attribute)\|	441880008 \|Congenital enlargement (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11300930023) - 36752001 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4977576029) - 36752001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5920735026) - 36752001 -> 441880008 (116676008) View
116676008 \|Associated morphology (attribute)\|	441880008 \|Congenital enlargement (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5920736025) - 36752001 -> 181279003 (363698007) View
363698007 \|Finding site (attribute)\|	181279003 \|Entire spleen (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6034075025) - 36752001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6074727022) - 36752001 -> 181279003 (363698007) View
363698007 \|Finding site (attribute)\|	181279003 \|Entire spleen (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10519232020) - 36752001 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4662753021) - 36752001 -> 441880008 (116676008) View
116676008 \|Associated morphology (attribute)\|	441880008 \|Congenital enlargement (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4662754026) - 36752001 -> 181279003 (363698007) View
363698007 \|Finding site (attribute)\|	181279003 \|Entire spleen (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4977577022) - 36752001 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4977578028) - 36752001 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (763591027) - 36752001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3365295023) - 36752001 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3365296024) - 36752001 -> 90141005 (116676008) View
116676008 \|Associated morphology (attribute)\|	90141005 \|Congenital hypertrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (763590026) - 36752001 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (763593029) - 36752001 -> 90141005 (116676008) View
116676008 \|Associated morphology (attribute)\|	90141005 \|Congenital hypertrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (763592023) - 36752001 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1673827022) - 36752001 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1997954028) - 36752001 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (207729021) - 36752001 -> 16294009 (116680003) View
116680003 \|Is a (attribute)\|	16294009 \|Splenomegaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (207730027) - 36752001 -> 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
16294009 View
16294009	Splenomegaly (disorder)	Lách to	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
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
771511005 View
771511005	Thrombocythemia with distal limb defect (disorder)	Thrombocythemia with distal limb defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
56118002 View
56118002	Congenital syphilitic splenomegaly (disorder)	Congenital syphilitic splenomegaly	900000000000073002 \|Sufficiently defined by necessary conditions 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 (14f40bd1-2772-5d29-8e76-3fbf1db1e10c) 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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