783254003: Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\...
• \Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome

Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3758297010	Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3758298017	Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3758299013	Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4437001000168116	Hereditary persistence of foetal haemoglobin with sickle cell disease syndrome	en	Synonym	Active	Case insensitive	SNOMED Clinical Terms Australian extension
3758300017	A rare genetic hemoglobinopathy characterized by generally mild clinical phenotype, high fetal hemoglobin levels and mild microcytosis and hypochromia. In some cases, acute sickle cell disease manifestations were reported, namely acute chest syndrome and acute pain crisis.	en	Definition	Active	Case sensitive	SNOMED CT core
3758301018	A rare genetic haemoglobinopathy characterised by generally mild clinical phenotype, high fetal haemoglobin levels and mild microcytosis and hypochromia. In some cases, acute sickle cell disease manifestations were reported, namely acute chest syndrome and acute pain crisis.	en	Definition	Active	Case sensitive	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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