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Terminology chevron_right Concepts chevron_right 234411007

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Component

234411007

The component that hold information about this concept.

Fully Specified Name (FSN)

Blood group deletion syndrome (disorder)

Shortest Term

Mcleod syndrome

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Blood group deletion syndrome (disorder)

SCTID: 234411007, Primitive, Active

234411007|Blood group deletion syndrome (disorder)|

en Blood group deletion syndrome
en Blood group deletion syndrome (disorder)
en Mcleod syndrome

Expression

234411007 |Blood group deletion syndrome (disorder)|
 <<< 234409003 |Erythrocyte membrane abnormality (disorder)| : 
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
351207014 - Blood group deletion syndrome (en) View
351207014	en	Synonym (core metadata concept)	Blood group deletion syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
622726012 - Blood group deletion syndrome (disorder) (en) View
622726012	en	Fully specified name (core metadata concept)	Blood group deletion syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1495080011 - McLeod syndrome (en) View
1495080011	en	Synonym (core metadata concept)	McLeod syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
351208016 - McCleod syndrome (en) View
351208016	en	Synonym (core metadata concept)	McCleod syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (514017026) - 234411007 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2712057023) - 234411007 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2253610020) - 234411007 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (514016024) - 234411007 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (48080027) - 234411007 -> 234409003 (116680003) View
116680003 \|Is a (attribute)\|	234409003 \|Erythrocyte membrane abnormality (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
234409003 View
234409003	Erythrocyte membrane abnormality (disorder)	Erythrocyte membrane abnormality	900000000000074008 \|Necessary but not sufficient concept 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 (9b3bd731-1f11-574f-9f56-8c07c4424e4d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D75.8	TRUE	ALWAYS D75.8	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)\|

Terminology chevron_right Concepts chevron_right 234411007

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