127042006: Sickle cell beta plus thalassemia (disorder)

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

\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 (disorder)\Hereditary hemoglobinopathy (disorder)\...

\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\...

\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia

\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia

\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\...

\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia

\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia

\Procedure related finding\Evaluation finding\...

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Beta plus thalassemia\Sickle cell beta plus thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia\Sickle cell beta plus thalassaemia

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
Sickle cell beta plus thalassaemia	Is a	Sickle cell-beta-thalassaemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell beta plus thalassaemia	Is a	Beta plus thalassemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell beta plus thalassaemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell beta plus thalassaemia	Causative agent (attribute)	Haemoglobin S	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell beta plus thalassaemia	Associated morphology	Drepanocyte (cell)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell beta plus thalassaemia	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell beta plus thalassaemia	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell beta plus thalassaemia	Has definitional manifestation	érythropénie	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell beta plus thalassaemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell beta plus thalassaemia	Associated morphology	Drepanocyte (cell)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell beta plus thalassaemia	Associated morphology	Drepanocyte (cell)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Sickle cell beta plus thalassaemia	Finding site	Erythroid cell (cell)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell beta plus thalassaemia	Finding site	Hematopoietic system structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell beta plus thalassaemia	Associated morphology	Drepanocyte (cell)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell beta plus thalassaemia	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Sickle cell beta plus thalassaemia	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Sickle cell beta plus thalassaemia	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Sickle cell beta plus thalassaemia	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Sickle cell beta plus thalassaemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Sickle cell beta plus thalassaemia	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3793686013	Sickle cell beta plus thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3793687016	Sickle cell beta plus thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3793688014	Sickle cell beta plus thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
330011	Sickle cell-beta^+^-thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
330011	Sickle cell-beta^+^-thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474035018	Sickle cell-beta^+^-thalassaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474035018	Sickle cell-beta^+^-thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
731081019	Sickle cell-beta^+^-thalassemia (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
731081019	Sickle cell-beta^+^-thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3793686013	Sickle cell beta plus thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3793687016	Sickle cell beta plus thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3793688014	Sickle cell beta plus thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core