127041004: Sickle cell-beta-thalassemia (disorder)

SNOMED CT Concept\Clinical 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\Hereditary hemoglobinopathy\...

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

\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia

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

\Thalassemia\Beta thalassemia\Sickle cell-beta-thalassemia
\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\...

\Beta thalassemia\Sickle cell-beta-thalassemia

\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-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\Sickle cell-beta-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\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-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\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Sickle cell-beta-thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Disorder of hematopoietic structure\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-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\Sickle cell-beta-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\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Sickle cell-beta-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-beta-thalassemia
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Sickle cell-beta-thalassemia
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease\Sickle cell-beta-thalassemia

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

Descriptions:

Id Description Lang Type Status Case? Module

329018 Sickle cell-beta-thalassemia en Synonym Active Entire term case insensitive SNOMED CT core module

474028014 Haemoglobin S/beta thalassaemia en Synonym Active Entire term case sensitive SNOMED CT core module

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

474030011 Thalassaemia with haemoglobin S disease en Synonym Active Only initial character case insensitive SNOMED CT core module

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

474032015 Hemoglobin S/beta thalassemia en Synonym Active Only initial character case insensitive SNOMED CT core module

474033013 Thalassemia with hemoglobin S disease en Synonym Active Only initial character case insensitive SNOMED CT core module

474034019 Sickle cell-beta-thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module

731080018 Sickle cell-beta-thalassemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell beta plus thalassemia	Is a	True	Sickle cell-beta-thalassemia	Inferred relationship	Existential restriction modifier
Sickle cell-beta^0^-thalassemia	Is a	True	Sickle cell-beta-thalassemia	Inferred relationship	Existential restriction modifier
Sickle cell-delta beta^0^-thalassemia	Is a	True	Sickle cell-beta-thalassemia	Inferred relationship	Existential restriction modifier
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with sickle cell beta-thalassaemia (situation)	Associated finding	True	Sickle cell-beta-thalassemia	Inferred relationship	Existential restriction modifier	1

This concept is not in any reference sets

Back to Start

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