127041004: Sickle cell-beta-thalassemia (disorder)

• SNOMED CT Concept\constatation clinique\...
• \Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...
• \troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\...
• \Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\...
• \Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\...
• \Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\affection du système hématopoïétique\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia
• \Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
• \Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\Sickle cell-beta-thalassemia
• \Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\thalassémie\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassemia

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
329018	Sickle cell-beta-thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474028014	Haemoglobin S/beta thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
474029018	Double heterozygous for Hb S and beta thalassaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474030011	Thalassaemia with haemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474031010	Double heterozygous for Hb S and beta thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474032015	Hemoglobin S/beta thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474033013	Thalassemia with hemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474034019	Sickle cell-beta-thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
731080018	Sickle cell-beta-thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

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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