127041004: Sickle cell-beta-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

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

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

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

\Beta thalassemia\Sickle cell-beta-thalassaemia

\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-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
\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
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-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
\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
\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
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Beta thalassemia\Sickle cell-beta-thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)\Sickle cell-thalassemia disease\Sickle cell-beta-thalassaemia

\Procedure related finding\Evaluation finding\...

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell beta plus thalassaemia	Is a	True	Sickle cell-beta-thalassaemia	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell-beta^0^-thalassemia (disorder)	Is a	True	Sickle cell-beta-thalassaemia	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell-delta beta^0^-thalassemia	Is a	True	Sickle cell-beta-thalassaemia	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
329018	Sickle cell-beta-thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474028014	Haemoglobin S/beta thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
474029018	Double heterozygous for Hb S and beta thalassaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474030011	Thalassaemia with haemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474031010	Double heterozygous for Hb S and beta thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474032015	Hemoglobin S/beta thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474033013	Thalassemia with hemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474034019	Sickle cell-beta-thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
731080018	Sickle cell-beta-thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
329018	Sickle cell-beta-thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
329018	Sickle cell-beta-thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474028014	Haemoglobin S/beta thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
474029018	Double heterozygous for Hb S and beta thalassaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474030011	Thalassaemia with haemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474031010	Double heterozygous for Hb S and beta thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474032015	Hemoglobin S/beta thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474033013	Thalassemia with hemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474034019	Sickle cell-beta-thalassaemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
474034019	Sickle cell-beta-thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
731080018	Sickle cell-beta-thalassemia (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
731080018	Sickle cell-beta-thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3454541001000118	Sichelzellkrankheit HbSbeta-Thal	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6958181000241113	drépanocytose-bêta-thalassémie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6958191000241110	bêta-thalassémie à hématies falciformes	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6958211000241114	HbS bêta-thalassémie	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6958181000241113	drépanocytose-bêta-thalassémie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6958191000241110	bêta-thalassémie à hématies falciformes	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6958211000241114	HbS bêta-thalassémie	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3454541001000118	Sichelzellkrankheit HbSbeta-Thal	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module