191201002: Hereditary persistence of fetal hemoglobin (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin
• \Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary persistence of fetal hemoglobin

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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

Expanded Value Set

This concept is not in any reference sets

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