934007: Thalassemia intermedia (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\Thalassaemia intermedia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia intermedia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia intermedia
• \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\Thalassaemia intermedia
• \Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia intermedia
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia intermedia
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia intermedia
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia intermedia

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2644018	Thalassemia intermedia	en	Synonym	Active	Case insensitive	SNOMED CT core
510307010	Thalassaemia intermedia	en	Synonym	Active	Case insensitive	SNOMED CT core
837127011	Thalassemia intermedia (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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