45028007: Elliptocyte (cell)

SNOMED CT Concept\Body structure\...

\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Body system structure\Hematological system structure (body structure)\Blood cell\Erythrocyte\Abnormal red blood cell\Poikilocyte (cell)\Elliptocyte (cell)

\Cell\Entire cell (cell)\...

\Erythroid cell (cell)\Erythrocyte\Abnormal red blood cell\Poikilocyte (cell)\Elliptocyte (cell)

\Blood cell\Erythrocyte\Abnormal red blood cell\Poikilocyte (cell)\Elliptocyte (cell)

\Abnormal cell\Abnormal red blood cell\Poikilocyte (cell)\Elliptocyte (cell)

\Morphologically altered structure\Morphologically abnormal structure\Abnormal cell\Abnormal red blood cell\Poikilocyte (cell)\Elliptocyte (cell)

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

Descriptions:

Id Description Lang Type Status Case? Module

75102016 Elliptocyte en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1772144018 Elliptocyte (cell) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

75102016 Elliptocyte en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

75102016 Elliptocyte en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

75103014 Ovalocyte en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

75103014 Ovalocyte en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

782222019 Elliptocyte (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1772144018 Elliptocyte (cell) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

1772144018 Elliptocyte (cell) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Elliptocyte (cell)	Is a	Abnormality of red blood cells	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Elliptocyte (cell)	Is a	Poikilocyte (cell)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Elliptocyte (cell)	partie de	Entire body as a whole (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Elliptocyte (cell)	partie de	Entire haematopoietic system	false	Additional relationship (core metadata concept)	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Oval macrocyte	Is a	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)
Pencil cell	Is a	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)
Elliptocytosis	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Ovalocyte	Is a	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to glycophorin C deficiency	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Hereditary elliptocytosis with transient poikilocytosis (disorder)	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Hereditary elliptocytosis	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Hereditary elliptocytosis due to deficiency of protein 4.1	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Hereditary elliptocytosis due to abnormal protein 4.1	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Hereditary elliptocytosis due to beta spectrin defect in self-association	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	9
Hereditary elliptocytosis due to alpha spectrin defect	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Homozygous hereditary elliptocytosis (disorder)	Associated morphology	True	Elliptocyte (cell)	Inferred relationship	Existential restriction modifier (core metadata concept)	1

This concept is not in any reference sets