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45028007: Elliptocyte (cell)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1772144018 Elliptocyte (cell) en Fully specified name Active Case insensitive SNOMED CT core
75102016 Elliptocyte en Synonym Active Case insensitive SNOMED CT core
75103014 Ovalocyte en Synonym Inactive Case insensitive SNOMED CT core
782222019 Elliptocyte (morphologic abnormality) en Fully specified name Inactive Initial character case insensitive SNOMED CT core

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Elliptocyte Is a Abnormality of red blood cells false Inferred relationship Some
Elliptocyte Is a Poikilocyte true Inferred relationship Some
Elliptocyte Part of Entire body as a whole false Inferred relationship Some
Elliptocyte Part of Entire haematopoietic system false Additional relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary elliptocytosis due to glycophorin C deficiency Associated morphology True Elliptocyte Inferred relationship Some 4
Hereditary elliptocytosis with transient poikilocytosis Associated morphology True Elliptocyte Inferred relationship Some 4
Hereditary elliptocytosis Associated morphology True Elliptocyte Inferred relationship Some 1
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Associated morphology True Elliptocyte Inferred relationship Some 4
Hereditary elliptocytosis due to deficiency of protein 4.1 Associated morphology True Elliptocyte Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 Associated morphology True Elliptocyte Inferred relationship Some 4
Hereditary elliptocytosis due to beta spectrin defect in self-association Associated morphology True Elliptocyte Inferred relationship Some 4
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome Associated morphology True Elliptocyte Inferred relationship Some 9
Hereditary elliptocytosis due to alpha spectrin defect Associated morphology True Elliptocyte Inferred relationship Some 4
Homozygous hereditary elliptocytosis Associated morphology True Elliptocyte Inferred relationship Some 1
Oval macrocyte Is a True Elliptocyte Inferred relationship Some
Pencil cell Is a True Elliptocyte Inferred relationship Some
Elliptocytosis Associated morphology True Elliptocyte Inferred relationship Some 1
Ovalocyte Is a True Elliptocyte Inferred relationship Some

Reference Sets

Body structure foundation reference set

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