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Terminology chevron_right Concepts chevron_right 205735005

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Component

205735005

The component that hold information about this concept.

Fully Specified Name (FSN)

Hypoplasia of spleen (disorder)

Shortest Term

Hypoplasia 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

Hypoplasia of spleen (disorder)

SCTID: 205735005, Defined, Active

205735005|Hypoplasia of spleen (disorder)|

en Hypoplasia of spleen
en Hypoplasia of spleen (disorder)

Expression

205735005 |Hypoplasia of spleen (disorder)|
 === 51244008 |Disorder of spleen (disorder)|
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 78961009 |Splenic structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
315505011 - Hypoplasia of spleen (en) View
315505011	en	Synonym (core metadata concept)	Hypoplasia of spleen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
591143011 - Hypoplasia of spleen (disorder) (en) View
591143011	en	Fully specified name (core metadata concept)	Hypoplasia of spleen (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (331076025) - 205735005 -> 57497006 (116680003) View
116680003 \|Is a (attribute)\|	57497006 \|Congenital anomaly of spleen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971836021) - 205735005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3437302024) - 205735005 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3442448020) - 205735005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4651096024) - 205735005 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4651097026) - 205735005 -> 51244008 (116680003) View
116680003 \|Is a (attribute)\|	51244008 \|Disorder of spleen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4651098020) - 205735005 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (971835020) - 205735005 -> 78961009 (363698007) View
363698007 \|Finding site (attribute)\|	78961009 \|Splenic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1791646020) - 205735005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971837028) - 205735005 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
93292008 View
93292008	Congenital hypoplasia of spleen (disorder)	Congenital microsplenia	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 (2e1f25fc-0e4f-5c52-a9df-1d2e925367fd) 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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