427306008: Hereditary hemoglobinopathy (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)

\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)
\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)

\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)
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)
\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)
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)
\Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2007. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2662307010 Hereditary hemoglobinopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2674112019 Hereditary hemoglobinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2674113012 Hereditary haemoglobinopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary hemoglobinopathy (disorder)	est un(e) (attribut)	Hemoglobinopathy	true	Inferred relationship	Some
Hereditary hemoglobinopathy (disorder)	est un(e) (attribut)	Hereditary red blood cell disorder (disorder)	true	Inferred relationship	Some
Hereditary hemoglobinopathy (disorder)	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
Hereditary hemoglobinopathy (disorder)	est défini par la manifestation de (attribut)	constatation à propos de la lignée rouge	false	Inferred relationship	Some
Hereditary hemoglobinopathy (disorder)	localisation d'une constatation (attribut)	Erythrocyte	false	Inferred relationship	Some
Hereditary hemoglobinopathy (disorder)	est un(e) (attribut)	Congenital disease	true	Inferred relationship	Some
Hereditary hemoglobinopathy (disorder)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Hereditary hemoglobinopathy (disorder)	localisation d'une constatation (attribut)	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Haemoglobinopathy Toms River	est un(e) (attribut)	True	Hereditary hemoglobinopathy (disorder)	Inferred relationship	Some
Homozygous hemoglobinopathy	est un(e) (attribut)	True	Hereditary hemoglobinopathy (disorder)	Inferred relationship	Some
thalassémie	est un(e) (attribut)	True	Hereditary hemoglobinopathy (disorder)	Inferred relationship	Some
Hereditary hemoglobinopathy due to globin chain mutation	est un(e) (attribut)	True	Hereditary hemoglobinopathy (disorder)	Inferred relationship	Some
Hereditary persistence of foetal haemoglobin	est un(e) (attribut)	True	Hereditary hemoglobinopathy (disorder)	Inferred relationship	Some
Heterozygous hemoglobinopathy	est un(e) (attribut)	True	Hereditary hemoglobinopathy (disorder)	Inferred relationship	Some

This concept is not in any reference sets