26682008: Homozygous beta thalassemia (disorder)

SNOMED CT Concept\constatation clinique\...

\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\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)

\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)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)

\anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)

\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)

\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)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Disease\anomalie des éléments figurés du sang (trouble)\troubles héréditaires des éléments figurés du sang\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Disease\anomalie des éléments figurés du sang (trouble)\anémie\Anemia due to disturbance of hemoglobin synthesis\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Disease\anomalie des éléments figurés du sang (trouble)\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\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)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Disease\affection d'un système corporel\anomalie de la lignée rouge\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)
\Disease\Congenital disease\Hereditary hemoglobinopathy (disorder)\thalassémie\Beta thalassemia (disorder)\bêtathalassémie homozygote (trouble)

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
bêtathalassémie homozygote (trouble)	interprète (attribut)	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
bêtathalassémie homozygote (trouble)	est un(e) (attribut)	Beta thalassemia (disorder)	true	Inferred relationship	Some
bêtathalassémie homozygote (trouble)	est défini par la manifestation de (attribut)	Erythropenia	false	Inferred relationship	Some
bêtathalassémie homozygote (trouble)	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
bêtathalassémie homozygote (trouble)	localisation d'une constatation (attribut)	structure d'un système corporel	false	Inferred relationship	Some
bêtathalassémie homozygote (trouble)	a pour interprétation (attribut)	au-dessous de l'étendue de référence	false	Inferred relationship	Some	1
bêtathalassémie homozygote (trouble)	interprète (attribut)	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
bêtathalassémie homozygote (trouble)	a pour interprétation (attribut)	au-dessous de l'étendue de référence	true	Inferred relationship	Some	2
bêtathalassémie homozygote (trouble)	interprète (attribut)	Red blood cell count	false	Inferred relationship	Some	2
bêtathalassémie homozygote (trouble)	survenue (attribut)	congénital	true	Inferred relationship	Some	3
bêtathalassémie homozygote (trouble)	localisation d'une constatation (attribut)	Erythrocyte	true	Inferred relationship	Some	3
bêtathalassémie homozygote (trouble)	localisation d'une constatation (attribut)	structure du système hématopoïétique	false	Inferred relationship	Some
bêtathalassémie homozygote (trouble)	localisation d'une constatation (attribut)	Erythrocyte	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
3391613014	bêta-thalassémie homozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
411111000241119	bêtathalassémie homozygote (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
44671012	Homozygous beta thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
44672017	Cooley's anemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
44673010	Mediterranean anemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
483318012	Beta thalassaemia major	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
483319016	Cooley's anaemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
483320010	Homozygous beta thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
596091000172115	bêtathalassémie homozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
757162012	Homozygous beta thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core