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36472007: Sickle cell-thalassemia disease (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
3035990017 Sickle cell thalassaemia disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3036285019 Sickle cell thalassemia disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
486462013 Sickle cell-thalassaemia disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
486463015 Haemoglobin S-F disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
486464014 Thalassaemia-haemoglobin S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
60878015 Hemoglobin S-F disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
60879011 Thalassemia-hemoglobin S disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
60880014 Sickle cell-thalassemia disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
60881013 Microdrepanocytic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
60882018 Microdrepanocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768228015 Sickle cell-thalassemia disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sickle cell-thalassaemia disease interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 3
Sickle cell-thalassaemia disease est un(e) (attribut) Sickle cell-hemoglobin SS disease false Inferred relationship Some
Sickle cell-thalassaemia disease est un(e) (attribut) Thalassaemia with other haemoglobinopathy true Inferred relationship Some
Sickle cell-thalassaemia disease localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some 1
Sickle cell-thalassaemia disease est défini par la manifestation de (attribut) Erythropenia false Inferred relationship Some
Sickle cell-thalassaemia disease morphologie associée (attribut) Drepanocyte (cell) false Inferred relationship Some 1
Sickle cell-thalassaemia disease morphologie associée (attribut) Drepanocyte (cell) false Inferred relationship Some 2
Sickle cell-thalassaemia disease est un(e) (attribut) Hereditary red blood cell disorder (disorder) false Inferred relationship Some
Sickle cell-thalassaemia disease est un(e) (attribut) affection du système hématopoïétique true Inferred relationship Some
Sickle cell-thalassaemia disease localisation d'une constatation (attribut) Erythroid cell (cell) false Inferred relationship Some 2
Sickle cell-thalassaemia disease est un(e) (attribut) Sickling disorder due to hemoglobin S (disorder) true Inferred relationship Some
Sickle cell-thalassaemia disease morphologie associée (attribut) Drepanocyte (cell) true Inferred relationship Some 1
Sickle cell-thalassaemia disease localisation d'une constatation (attribut) structure du système hématopoïétique true Inferred relationship Some 1
Sickle cell-thalassaemia disease a pour interprétation (attribut) au-dessous de l'étendue de référence false Inferred relationship Some 2
Sickle cell-thalassaemia disease a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 3
Sickle cell-thalassaemia disease interprète (attribut) Measurement of total haemoglobin concentration false Inferred relationship Some 2
Sickle cell-thalassaemia disease interprète (attribut) Red blood cell count false Inferred relationship Some 3
Sickle cell-thalassaemia disease survenue (attribut) congénital true Inferred relationship Some 4
Sickle cell-thalassaemia disease localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 4
Sickle cell-thalassaemia disease morphologie associée (attribut) Drepanocyte (cell) false Inferred relationship Some 1
Sickle cell-thalassaemia disease localisation d'une constatation (attribut) Erythrocyte false Inferred relationship Some
Sickle cell-thalassaemia disease Causative agent Haemoglobin S false Inferred relationship Some
Sickle cell-thalassaemia disease localisation d'une constatation (attribut) Entire hematological system (body structure) false Inferred relationship Some 1
Sickle cell-thalassaemia disease localisation d'une constatation (attribut) structure du système hématopoïétique false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Sickle cell-beta-thalassemia est un(e) (attribut) True Sickle cell-thalassaemia disease Inferred relationship Some
Sickle cell-delta beta^0^-thalassemia est un(e) (attribut) False Sickle cell-thalassaemia disease Inferred relationship Some
Sickle cell anemia with coexistent alpha-thalassemia est un(e) (attribut) True Sickle cell-thalassaemia disease Inferred relationship Some
Sickle cell trait with coexistent alpha-thalassemia est un(e) (attribut) False Sickle cell-thalassaemia disease Inferred relationship Some
Sickle cell-thalassemia disease with crisis (disorder) est un(e) (attribut) True Sickle cell-thalassaemia disease Inferred relationship Some
Sickle cell-thalassemia disease without crisis (disorder) est un(e) (attribut) True Sickle cell-thalassaemia disease Inferred relationship Some

Reference Sets

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

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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