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19442009: heterozygote thalassemie (aandoening)

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

\Laboratory test finding (finding)\Hematopoietic system finding\...

\Haematology test outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Heterozygous thalassemia

\Hemoglobin finding\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Heterozygous thalassemia

\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)\Thalassemia\Heterozygous thalassemia

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Heterozygous thalassemia

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Heterozygous thalassemia
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Heterozygous thalassemia

\Procedure related finding\Evaluation finding\...

\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\Heterozygous thalassemia
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Heterozygous thalassemia
\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\Heterozygous thalassemia
\Disease\Disorder of cellular component of blood (disorder)\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Heterozygous thalassemia
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Heterozygous thalassemia
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Heterozygous thalassemia
\Disease\Disorder of body system\Hematological disorder (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Heterozygous thalassemia
\Disease\Disorder of body system\Hematological disorder (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Heterozygous thalassemia
\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\Heterozygous thalassemia

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
Heterozygous thalassemia	Is a	Thalassemia	true	Inferred relationship	Some
Heterozygous thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Heterozygous thalassemia	Finding site	Erythrocyte	false	Inferred relationship	Some
Heterozygous thalassemia	Has definitional manifestation	erytropenie (bevinding)	false	Inferred relationship	Some
Heterozygous thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Heterozygous thalassemia	Finding site	Body system structure	false	Inferred relationship	Some
Heterozygous thalassemia	Has interpretation	Below reference range	false	Inferred relationship	Some	1
Heterozygous thalassemia	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
Heterozygous thalassemia	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Heterozygous thalassemia	Interprets	Red blood cell count	false	Inferred relationship	Some	2
Heterozygous thalassemia	Occurrence	Congenital	true	Inferred relationship	Some	3
Heterozygous thalassemia	Finding site	Erythrocyte	true	Inferred relationship	Some	3
Heterozygous thalassemia	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Beta thalassaemia trait	Is a	True	Heterozygous thalassemia	Inferred relationship	Some
Thalassemia minor	Is a	False	Heterozygous thalassemia	Inferred relationship	Some
Alpha trait thalassemia	Is a	True	Heterozygous thalassemia	Inferred relationship	Some
Thalassemia minor NEC	Is a	False	Heterozygous thalassemia	Inferred relationship	Some
Delta beta thalassemia trait (disorder)	Is a	True	Heterozygous thalassemia	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
32747012	Heterozygous thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
32748019	Heterozygous thalassemia, NOS	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
32749010	Thalassemia trait, NOS	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
32750010	Thalassemia trait	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
479508018	Heterozygous thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
479509014	Thalassaemia trait	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
747569017	Heterozygous thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2770070012	Thalassaemia minor	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2771433018	Thalassemia minor	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
341671000146117	heterozygote thalassemie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
341681000146115	heterozygote thalassemie (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)