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191169008: Hereditary elliptocytosis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
293982012 Hereditary ovalocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
293983019 HE - Hereditary elliptocytosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
293984013 Hereditary elliptocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3787598014 Congenital elliptocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
524041000241119 elliptocytose familiale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
574836013 Hereditary elliptocytosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
886781000172116 elliptocytose familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
960061000172116 EH - elliptocytose héréditaire fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary elliptocytosis survenue (attribut) congénital true Inferred relationship Some 1
Hereditary elliptocytosis interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 3
Hereditary elliptocytosis interprète (attribut) Hemolysis (observable entity) true Inferred relationship Some 4
Hereditary elliptocytosis est un(e) (attribut) Congenital haemolytic anaemia true Inferred relationship Some
Hereditary elliptocytosis interprète (attribut) Red blood cell count true Inferred relationship Some 2
Hereditary elliptocytosis a pour interprétation (attribut) présent (valeur de l'attribut) true Inferred relationship Some 4
Hereditary elliptocytosis a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
Hereditary elliptocytosis est un(e) (attribut) anémie hémolytique héréditaire true Inferred relationship Some
Hereditary elliptocytosis est un(e) (attribut) Congenital malformation true Inferred relationship Some
Hereditary elliptocytosis a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 3
Hereditary elliptocytosis Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Hereditary elliptocytosis morphologie associée (attribut) Elliptocyte (cell) true Inferred relationship Some 1
Hereditary elliptocytosis est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Hereditary elliptocytosis est un(e) (attribut) Erythrocyte membrane abnormality true Inferred relationship Some
Hereditary elliptocytosis localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary elliptocytosis est un(e) (attribut) Hereditary red blood cell disorder (disorder) false Inferred relationship Some
Hereditary elliptocytosis localisation d'une constatation (attribut) structure d'un système corporel false Inferred relationship Some
Hereditary elliptocytosis est défini par la manifestation de (attribut) constatation à propos de la lignée rouge false Inferred relationship Some
Hereditary elliptocytosis localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Hereditary elliptocytosis localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Homozygous hereditary elliptocytosis (disorder) est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some
Hereditary elliptocytosis due to glycophorin C deficiency est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some
Hereditary elliptocytosis due to beta spectrin defect in self-association est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some
Hereditary elliptocytosis due to abnormal protein 4.1 est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some
Hereditary elliptocytosis with transient poikilocytosis est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some
Hereditary elliptocytosis due to alpha spectrin defect est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) est un(e) (attribut) True Hereditary elliptocytosis Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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