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63599005: Acanthocyte (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
105695018 Acanthocyte en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
105696017 Acanthrocyte en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
105697014 Crenated cell en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
105698016 Spur cell en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1772297017 Acanthocyte (cell) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1788101016 Spiny prickle cell en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acanthocyte Is a Abnormality of red blood cells false Inferred relationship Some
Acanthocyte Is a Poikilocytosis false Inferred relationship Some
Acanthocyte Is a Poikilocyte (cell) true Inferred relationship Some
Acanthocyte partie de Entire body as a whole false Inferred relationship Some
Acanthocyte partie de Entire hematopoietic system false Additional relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary acanthocytosis Associated morphology True Acanthocyte Inferred relationship Some 1
Chorea acanthocytosis syndrome Associated morphology True Acanthocyte Inferred relationship Some 1
Acanthocytosis Associated morphology True Acanthocyte Inferred relationship Some 1
A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia). Associated morphology False Acanthocyte Inferred relationship Some 2
McLeod neuroacanthocytosis syndrome (MLS) is a form of neuroacanthocytosis and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens. Associated morphology True Acanthocyte Inferred relationship Some 2

This concept is not in any reference sets

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