191201002: Hereditary persistence of fetal hemoglobin (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
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin
• \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
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin
• \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
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary persistence of fetal haemoglobin

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2793120016	Hereditary persistence of foetal haemoglobin	en	Synonym	Active	Case insensitive	SNOMED CT core
2793720014	HPFH - Hereditary persistence of foetal haemoglobin	en	Synonym	Active	Case sensitive	SNOMED CT core
294068017	Hb F disease	en	Synonym	Active	Case sensitive	SNOMED CT core
294069013	HPFH - Hereditary persistence of fetal hemoglobin	en	Synonym	Active	Case sensitive	SNOMED CT core
294070014	Hereditary persistence of fetal hemoglobin	en	Synonym	Active	Case insensitive	SNOMED CT core
294071013	HPFH - Hereditary persistence of fetal haemoglobin	en	Synonym	Active	Case sensitive	SNOMED CT core
294072018	Hereditary persistence of fetal haemoglobin	en	Synonym	Active	Case insensitive	SNOMED CT core
574873011	Hereditary persistence of fetal hemoglobin (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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