79592006: Beta plus thalassemia (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Finding of substance level\Finding of protein level\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Evaluation finding\Hematopoietic system finding\Hematology test outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Beta plus thalassemia

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

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Beta plus thalassemia

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Beta plus thalassemia

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Beta plus thalassemia	Is a	Beta thalassemia	true	Inferred relationship	Existential restriction modifier
Beta plus thalassemia	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Beta plus thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Beta plus thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Beta plus thalassemia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Beta plus thalassemia	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Beta plus thalassemia	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Beta plus thalassemia	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Beta plus thalassemia	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Beta plus thalassemia	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	2
Beta plus thalassemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Beta plus thalassemia	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Beta plus thalassemia	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell beta plus thalassemia	Is a	True	Beta plus thalassemia	Inferred relationship	Existential restriction modifier
beta^+^ Thalassemia, normal Hb A>2<, type 2	Is a	True	Beta plus thalassemia	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia	Is a	True	Beta plus thalassemia	Inferred relationship	Existential restriction modifier
Beta plus thalassemia normal hemoglobin A>2< type 1 silent	Is a	True	Beta plus thalassemia	Inferred relationship	Existential restriction modifier
Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia	Is a	True	Beta plus thalassemia	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
132046013	beta^+^ Thalassemia	en	Synonym	Inactive	Entire term case sensitive	SNOMED CT core module
132047016	beta^+^ Thalassemia, NOS	en	Synonym	Inactive	Only initial character case insensitive	SNOMED CT core module
504149012	Beta + thalassemia	en	Synonym	Inactive	Entire term case insensitive	SNOMED CT core module
504150012	beta^+^ Thalassaemia	en	Synonym	Inactive	Entire term case sensitive	SNOMED CT core module
504151011	Beta + thalassaemia	en	Synonym	Inactive	Entire term case insensitive	SNOMED CT core module
820659012	beta^+^ Thalassemia (disorder)	en	Fully specified name	Inactive	Entire term case sensitive	SNOMED CT core module
3036536013	Beta plus thalassemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3036564015	Beta plus thalassaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3793603015	Beta plus thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3800343016	beta plus thalassaemia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3800344010	beta plus thalassemia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module