191201002: Hereditary persistence of fetal hemoglobin (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood (disorder)\...

\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of fetal hemoglobin

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of fetal hemoglobin
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of fetal hemoglobin

\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)\Hereditary persistence of fetal hemoglobin
\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)\Hereditary persistence of fetal hemoglobin
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of fetal hemoglobin
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of fetal hemoglobin
\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)\Hereditary persistence of fetal hemoglobin
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of fetal hemoglobin
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of fetal hemoglobin
\Disease\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of fetal hemoglobin

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary persistence of fetal hemoglobin	Is a	Hemoglobinopathy	false	Inferred relationship	Some
Hereditary persistence of fetal hemoglobin	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Hereditary persistence of fetal hemoglobin	Finding site	Erythrocyte	false	Inferred relationship	Some
Hereditary persistence of fetal hemoglobin	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Hereditary persistence of fetal hemoglobin	Is a	Hereditary red blood cell disorder (disorder)	false	Inferred relationship	Some
Hereditary persistence of fetal hemoglobin	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Hereditary persistence of fetal hemoglobin	Finding site	Body system structure	false	Inferred relationship	Some
Hereditary persistence of fetal hemoglobin	Is a	Hereditary hemoglobinopathy (disorder)	true	Inferred relationship	Some
Hereditary persistence of fetal hemoglobin	Occurrence	Congenital	true	Inferred relationship	Some	1
Hereditary persistence of fetal hemoglobin	Finding site	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome	Is a	True	Hereditary persistence of fetal hemoglobin	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
294068017	Hb F disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
294069013	HPFH - Hereditary persistence of fetal hemoglobin	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
294070014	Hereditary persistence of fetal hemoglobin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
294071013	HPFH - Hereditary persistence of fetal haemoglobin	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
294072018	Hereditary persistence of fetal haemoglobin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
574873011	Hereditary persistence of fetal hemoglobin (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2793120016	Hereditary persistence of foetal haemoglobin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2793720014	HPFH - Hereditary persistence of foetal haemoglobin	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
11462211000172112	hémoglobine fœtale persistante	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
5098251000172115	HPFH	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
5098261000172118	erfelijke persistentie van HbF	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
5098271000172110	hereditaire persistentie van foetaal hemoglobine	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)