85557000: Hereditary persistence of fetal hemoglobin deletion type (disorder)

• SNOMED CT Concept\Clinical finding (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 (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Procedure related finding\Evaluation finding\...
• \Measurement finding\Finding of substance level (finding)\Finding of protein level (finding)\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\Hereditary persistence of foetal haemoglobin (HPFH) deletion type

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
141806018	HPFH deletion type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2621336012	Hereditary persistence of fetal hemoglobin (HPFH) deletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2795252012	Hereditary persistence of foetal haemoglobin (HPFH) deletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2913396019	Hereditary persistence of fetal hemoglobin deletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2913799012	Hereditary persistence of fetal hemoglobin deletion type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3013769014	Hereditary persistence of fetal haemoglobin deletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
141806018	HPFH deletion type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
827635016	HPFH deletion type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
827635016	HPFH deletion type (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2612758012	Hereditary persistence of fetal hemoglobin (HPFH) deletion type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2621336012	Hereditary persistence of fetal hemoglobin (HPFH) deletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2621337015	Hereditary persistence of fetal haemoglobin (HPFH) deletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2795252012	Hereditary persistence of foetal haemoglobin (HPFH) deletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2913396019	Hereditary persistence of fetal hemoglobin deletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2913396019	Hereditary persistence of fetal hemoglobin deletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2913799012	Hereditary persistence of fetal hemoglobin deletion type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2913799012	Hereditary persistence of fetal hemoglobin deletion type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3013769014	Hereditary persistence of fetal haemoglobin deletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3013769014	Hereditary persistence of fetal haemoglobin deletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6260871000241111	persistance héréditaire d'hémoglobine fœtale de type délétion	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6260881000241113	PHHF (persistance héréditaire d'hémoglobine fœtale) de type délétion	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6260871000241111	persistance héréditaire d'hémoglobine fœtale de type délétion	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6260881000241113	PHHF (persistance héréditaire d'hémoglobine fœtale) de type délétion	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Description inactivation indicator reference set

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