127041004: Sickle cell-beta-thalassemia (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of blood, lymphatics and immune system\Blood disease\...

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\...

\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\...

\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia

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

\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia

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

\Beta thalassaemia\Sickle cell-beta-thalassaemia

\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Disorder of haematopoietic structure\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia
\Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassaemia
\Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Beta thalassaemia\Sickle cell-beta-thalassaemia
\Disease\Congenital disease\Hereditary haemoglobinopathy\Thalassaemia\Thalassaemia with other haemoglobinopathy\Sickle cell-thalassaemia disease\Sickle cell-beta-thalassaemia

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

329018 Sickle cell-beta-thalassemia en Synonym Active Case insensitive SNOMED CT core

474028014 Haemoglobin S/beta thalassaemia en Synonym Active Case sensitive SNOMED CT core

474029018 Double heterozygous for Hb S and beta thalassaemia en Synonym Active Initial character case insensitive SNOMED CT core

474030011 Thalassaemia with haemoglobin S disease en Synonym Active Initial character case insensitive SNOMED CT core

474031010 Double heterozygous for Hb S and beta thalassemia en Synonym Active Initial character case insensitive SNOMED CT core

474032015 Hemoglobin S/beta thalassemia en Synonym Active Initial character case insensitive SNOMED CT core

474033013 Thalassemia with hemoglobin S disease en Synonym Active Initial character case insensitive SNOMED CT core

474034019 Sickle cell-beta-thalassaemia en Synonym Active Case insensitive SNOMED CT core

731080018 Sickle cell-beta-thalassemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sickle cell-beta-thalassaemia	Is a	Sickle cell-thalassaemia disease	true	Inferred relationship	Some
Sickle cell-beta-thalassaemia	Finding site	Haematopoietic system structure	false	Inferred relationship	Some	1
Sickle cell-beta-thalassaemia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Sickle cell-beta-thalassaemia	Associated morphology	Drepanocyte	false	Inferred relationship	Some	1
Sickle cell-beta-thalassaemia	Associated morphology	Drepanocyte	false	Inferred relationship	Some	2
Sickle cell-beta-thalassaemia	Finding site	Erythroid cell	false	Inferred relationship	Some	1
Sickle cell-beta-thalassaemia	Is a	Double heterozygous sickling disorder	true	Inferred relationship	Some
Sickle cell-beta-thalassaemia	Is a	Beta thalassaemia	true	Inferred relationship	Some
Sickle cell-beta-thalassaemia	Finding site	Haematopoietic system structure	true	Inferred relationship	Some	1
Sickle cell-beta-thalassaemia	Associated morphology	Drepanocyte	true	Inferred relationship	Some	1
Sickle cell-beta-thalassaemia	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Sickle cell-beta-thalassaemia	Has interpretation	Below reference range	false	Inferred relationship	Some	3
Sickle cell-beta-thalassaemia	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
Sickle cell-beta-thalassaemia	Interprets	Red blood cell count	false	Inferred relationship	Some	3
Sickle cell-beta-thalassaemia	Finding site	Entire haematological system	false	Inferred relationship	Some	1
Sickle cell-beta-thalassaemia	Finding site	Erythrocyte	false	Inferred relationship	Some
Sickle cell-beta-thalassaemia	Associated morphology	Drepanocyte	false	Inferred relationship	Some	1
Sickle cell-beta-thalassaemia	Causative agent	Haemoglobin S	false	Inferred relationship	Some
Sickle cell-beta-thalassaemia	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Sickle cell-beta-thalassaemia	Occurrence	Congenital	true	Inferred relationship	Some	4
Sickle cell-beta-thalassaemia	Finding site	Erythrocyte	true	Inferred relationship	Some	4

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell beta plus thalassaemia	Is a	True	Sickle cell-beta-thalassaemia	Inferred relationship	Some
Sickle cell-beta^0^-thalassaemia	Is a	True	Sickle cell-beta-thalassaemia	Inferred relationship	Some
Sickle cell-delta beta^0^-thalassaemia	Is a	True	Sickle cell-beta-thalassaemia	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
329018	Sickle cell-beta-thalassemia	en	Synonym	Active	Case insensitive	SNOMED CT core
474028014	Haemoglobin S/beta thalassaemia	en	Synonym	Active	Case sensitive	SNOMED CT core
474029018	Double heterozygous for Hb S and beta thalassaemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
474030011	Thalassaemia with haemoglobin S disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
474031010	Double heterozygous for Hb S and beta thalassemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
474032015	Hemoglobin S/beta thalassemia	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
474033013	Thalassemia with hemoglobin S disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
474034019	Sickle cell-beta-thalassaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
731080018	Sickle cell-beta-thalassemia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core