56205004: Hereditary persistence of fetal hemoglobin, nondeletion type (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\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \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\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\HPFH nondeletion type

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2612517019	Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type (disorder)	en	Fully specified name	Inactive	Initial character case insensitive	SNOMED CT core
2621002013	Hereditary persistence of fetal haemoglobin (HPFH) nondeletion type	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2621003015	Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2795474016	Hereditary persistence of foetal haemoglobin (HPFH) nondeletion type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2968752016	Hereditary persistence of fetal hemoglobin, nondeletion type	en	Synonym	Active	Case insensitive	SNOMED CT core
2968817015	Hereditary persistence of fetal hemoglobin, nondeletion type (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
794692016	HPFH nondeletion type (disorder)	en	Fully specified name	Inactive	Case sensitive	SNOMED CT core
93465016	HPFH nondeletion type	en	Synonym	Active	Case sensitive	SNOMED CT core
93466015	HPFH nondeletion type, NOS	en	Synonym	Inactive	Initial character 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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