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234409003: Erythrocyte membrane abnormality (disorder)


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
351205018 Erythrocyte membrane abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
622723016 Erythrocyte membrane abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


31 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrocyte membrane abnormality localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Erythrocyte membrane abnormality est défini par la manifestation de (attribut) constatation à propos de la lignée rouge false Inferred relationship Some
Erythrocyte membrane abnormality est un(e) (attribut) anomalie de la lignée rouge true Inferred relationship Some
Erythrocyte membrane abnormality localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 1
Erythrocyte membrane abnormality localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital elliptocytosis est un(e) (attribut) False Erythrocyte membrane abnormality Inferred relationship Some
Hereditary elliptocytosis est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
syndrome de déficit Rh (trouble) est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
Phosphatidylcholine-sterol acyltransferase deficiency (disorder) est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
sphérocytose héréditaire est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
Hereditary pyropoikilocytosis est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
Hereditary elliptocytosis with transient poikilocytosis est un(e) (attribut) False Erythrocyte membrane abnormality Inferred relationship Some
Blood group deletion syndrome est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
Abnormal cation transport syndrome est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
Alpha/beta lipoproteinemia est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
Lecithin cholesterol acyltransferase deficiency est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some
March hemoglobinuria est un(e) (attribut) False Erythrocyte membrane abnormality Inferred relationship Some
Hereditary acanthocytosis est un(e) (attribut) True Erythrocyte membrane abnormality Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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