19442009: Heterozygous thalassemia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Measurement finding\Finding of substance level\Protein level - finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Heterozygous thalassaemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Heterozygous thalassaemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Heterozygous thalassaemia
• \Evaluation finding\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Heterozygous thalassaemia
• \Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Heterozygous thalassaemia
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Heterozygous thalassaemia
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Heterozygous thalassaemia
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Heterozygous thalassaemia

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2770070012	Thalassaemia minor	en	Synonym	Active	Case insensitive	SNOMED CT core
2771433018	Thalassemia minor	en	Synonym	Active	Case insensitive	SNOMED CT core
32747012	Heterozygous thalassemia	en	Synonym	Active	Case insensitive	SNOMED CT core
32748019	Heterozygous thalassemia, NOS	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
32749010	Thalassemia trait, NOS	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
32750010	Thalassemia trait	en	Synonym	Active	Case insensitive	SNOMED CT core
479508018	Heterozygous thalassaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
479509014	Thalassaemia trait	en	Synonym	Active	Case insensitive	SNOMED CT core
747569017	Heterozygous thalassemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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