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45028007: Elliptocyte (cell)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
75102016 Elliptocyte en Synonym Active Entire term case insensitive SNOMED CT core module
1772144018 Elliptocyte (cell) en Fully specified name Active Entire term case insensitive SNOMED CT core module

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

This concept is not in any reference sets

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