61395005: Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (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\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \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\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Evaluation finding\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Haemoglobin low\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\...
• \Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\...
• \Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \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 G gamma beta plus thalassaemia
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Beta plus thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
• \Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Hereditary persistence of fetal haemoglobin thalassaemia\Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
102000014	HPFH G gamma beta^+^ thalassemia	en	Synonym	Inactive	Case sensitive	SNOMED CT core
2612458011	Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia (disorder)	en	Fully specified name	Inactive	Initial character case insensitive	SNOMED CT core
2620925018	Hereditary persistence of fetal haemoglobin (HPFH) G gamma beta^+^ thalassaemia	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2620926017	Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2793196016	Hereditary persistence of foetal haemoglobin (HPFH) G gamma beta^+^ thalassaemia	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2914079019	Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2915152013	Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia (disorder)	en	Fully specified name	Inactive	Initial character case insensitive	SNOMED CT core
3793694018	Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3793695017	Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3793698015	Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3800043011	HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia	en	Synonym	Active	Case sensitive	SNOMED CT core
3800044017	HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia	en	Synonym	Active	Case sensitive	SNOMED CT core
3800045016	HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia	en	Synonym	Active	Case sensitive	SNOMED CT core
498999014	HPFH G gamma beta^+^ thalassaemia	en	Synonym	Inactive	Case sensitive	SNOMED CT core
800452017	HPFH G gamma beta^+^ thalassemia (disorder)	en	Fully specified name	Inactive	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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