56205004: Hereditary persistence of fetal hemoglobin, nondeletion 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\HPFH nondeletion type
• \Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH nondeletion type
• \Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH nondeletion type
• \Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH nondeletion 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\HPFH nondeletion 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\HPFH nondeletion 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\HPFH nondeletion 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\HPFH nondeletion 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\HPFH nondeletion 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\HPFH nondeletion type
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH nondeletion 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\HPFH nondeletion type
• \Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH nondeletion 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\HPFH nondeletion type
• \Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH nondeletion 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\HPFH nondeletion 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\HPFH nondeletion type
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH nondeletion 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
93465016	HPFH nondeletion type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2621003015	Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2795474016	Hereditary persistence of foetal haemoglobin (HPFH) nondeletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2968752016	Hereditary persistence of fetal hemoglobin, nondeletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2968817015	Hereditary persistence of fetal hemoglobin, nondeletion type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
93465016	HPFH nondeletion type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
794692016	HPFH nondeletion type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
794692016	HPFH nondeletion type (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2612517019	Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2621002013	Hereditary persistence of fetal haemoglobin (HPFH) nondeletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2621003015	Hereditary persistence of fetal hemoglobin (HPFH) nondeletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2795474016	Hereditary persistence of foetal haemoglobin (HPFH) nondeletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2968752016	Hereditary persistence of fetal hemoglobin, nondeletion type	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2968752016	Hereditary persistence of fetal hemoglobin, nondeletion type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2968752016	Hereditary persistence of fetal hemoglobin, nondeletion type	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2968817015	Hereditary persistence of fetal hemoglobin, nondeletion type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2968817015	Hereditary persistence of fetal hemoglobin, nondeletion type (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6270171000241110	persistance héréditaire d'hémoglobine fœtale de type non délétion	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6270181000241112	PHHF (persistance héréditaire d'hémoglobine fœtale) de type non délétion	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6270171000241110	persistance héréditaire d'hémoglobine fœtale de type non délétion	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6270181000241112	PHHF (persistance héréditaire d'hémoglobine fœtale) de type non délétion	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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