32855007: Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Disorder of cellular component of blood (disorder)\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster
• \Disease\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Hereditary persistence of fetal hemoglobin thalassemia\HPFH unlinked to beta-globulin gene cluster

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
54830012	HPFH unlinked to beta-globulin gene cluster	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2620581019	Hereditary persistence of fetal hemoglobin (HPF) unlinked to beta-globulin gene cluster	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2793477014	Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2913546016	Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2914016017	Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3014153015	Hereditary persistence of fetal haemoglobin unlinked to beta-globulin gene cluster	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3330921000052112	hereditär persistens av fetalt hemoglobin utan koppling till betaglobulingenkluster	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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