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Terminology chevron_right Concepts chevron_right 234409003

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Component

234409003

The component that hold information about this concept.

Fully Specified Name (FSN)

Erythrocyte membrane abnormality (disorder)

Shortest Term

Erythrocyte membrane abnormality

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

Erythrocyte membrane abnormality (disorder)

SCTID: 234409003, Primitive, Active

234409003|Erythrocyte membrane abnormality (disorder)|

en Erythrocyte membrane abnormality
en Erythrocyte membrane abnormality (disorder)

Expression

234409003 |Erythrocyte membrane abnormality (disorder)|
 <<< 38292009 |Red blood cell disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
351205018 - Erythrocyte membrane abnormality (en) View
351205018	en	Synonym (core metadata concept)	Erythrocyte membrane abnormality	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
622723016 - Erythrocyte membrane abnormality (disorder) (en) View
622723016	en	Fully specified name (core metadata concept)	Erythrocyte membrane abnormality (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (514010029) - 234409003 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2712054027) - 234409003 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2253608023) - 234409003 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (514011025) - 234409003 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (48076021) - 234409003 -> 38292009 (116680003) View
116680003 \|Is a (attribute)\|	38292009 \|Red blood cell disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
38292009 View
38292009	Red blood cell disorder (disorder)	Red blood cell disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
191169008 View
191169008	Hereditary elliptocytosis (disorder)	Hereditary ovalocytosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11376001 View
11376001	Hereditary acanthocytosis (disorder)	Hereditary acanthocytosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
37272000 View
37272000	Rh deficiency syndrome (disorder)	Rh deficiency syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
55995005 View
55995005	Hereditary spherocytosis (disorder)	Familial spherocytosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234411007 View
234411007	Blood group deletion syndrome (disorder)	Mcleod syndrome	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 (4f30984e-f4d4-5a4a-9a99-9fad9c65dfa9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	R71	TRUE	ALWAYS R71	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 234409003

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