191201002: Hereditary persistence of fetal hemoglobin (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation à propos du sang, des lymphatiques et du système immunitaire\anomalie des éléments figurés du sang (trouble)\...

\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin

\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin
\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin
\Disease\affection d'un système corporel\Hereditary disorder by system\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin
\Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary persistence of foetal haemoglobin

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 foetal haemoglobin	est un(e) (attribut)	Hemoglobinopathy	false	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	est un(e) (attribut)	Hereditary red blood cell disorder (disorder)	false	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	est défini par la manifestation de (attribut)	constatation à propos de la lignée rouge	false	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	est un(e) (attribut)	Hereditary hemoglobinopathy (disorder)	true	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	localisation d'une constatation (attribut)	Erythrocyte	false	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Hereditary persistence of foetal haemoglobin	localisation d'une constatation (attribut)	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome	est un(e) (attribut)	True	Hereditary persistence of foetal haemoglobin	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
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
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