85557000: Hereditary persistence of fetal hemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion type
• \Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion type
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion type
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion type
• \Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion type
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion type
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion 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\Hereditary persistence of fetal haemoglobin deletion type
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion type
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion type
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin deletion type

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
141806018	HPFH deletion type	en	Synonym	Active	Case sensitive	SNOMED CT core
2621336012	Hereditary persistence of fetal hemoglobin (HPFH) deletion type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2795252012	Hereditary persistence of foetal haemoglobin (HPFH) deletion type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2913396019	Hereditary persistence of fetal hemoglobin deletion type	en	Synonym	Active	Case insensitive	SNOMED CT core
2913799012	Hereditary persistence of fetal hemoglobin deletion type (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3013769014	Hereditary persistence of fetal haemoglobin deletion type	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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