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42601008: Congenital hemolytic anemia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
493386016 Congenital haemolytic anaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
71069015 Congenital hemolytic anemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
779519013 Congenital hemolytic anemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


11 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital haemolytic anaemia a pour interprétation (attribut) présent (valeur de l'attribut) true Inferred relationship Some 4
Congenital haemolytic anaemia interprète (attribut) Hemolysis (observable entity) true Inferred relationship Some 4
Congenital haemolytic anaemia est un(e) (attribut) anomalie de la lignée rouge true Inferred relationship Some
Congenital haemolytic anaemia est un(e) (attribut) Congenital anemia true Inferred relationship Some
Congenital haemolytic anaemia est un(e) (attribut) Hemolytic anemia true Inferred relationship Some
Congenital haemolytic anaemia localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Congenital haemolytic anaemia est défini par la manifestation de (attribut) Erythropenia false Inferred relationship Some
Congenital haemolytic anaemia est défini par la manifestation de (attribut) Hemolysis false Inferred relationship Some
Congenital haemolytic anaemia est un(e) (attribut) Hemolytic disorder false Inferred relationship Some
Congenital haemolytic anaemia localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some
Congenital haemolytic anaemia survenue (attribut) congénital true Inferred relationship Some 1
Congenital haemolytic anaemia localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 1
Congenital haemolytic anaemia interprète (attribut) Erythrocyte destruction, function (observable entity) false Inferred relationship Some
Congenital haemolytic anaemia a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
Congenital haemolytic anaemia a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 3
Congenital haemolytic anaemia interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 2
Congenital haemolytic anaemia interprète (attribut) Red blood cell count true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary elliptocytosis est un(e) (attribut) True Congenital haemolytic anaemia Inferred relationship Some
sphérocytose héréditaire est un(e) (attribut) False Congenital haemolytic anaemia Inferred relationship Some
Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism est un(e) (attribut) True Congenital haemolytic anaemia Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

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