36472007: Sickle cell-thalassemia disease (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\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\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\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\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\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\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\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease

\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

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

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease

\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
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\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
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease

\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
\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
\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
\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
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\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
\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
\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
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Disease\Disorder of body system\Disorder of hematopoietic structure\Sickle cell-thalassemia disease
\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
\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
\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
\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
\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
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\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
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease

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
Sickle cell-thalassemia disease	Is a	Sickle cell-hemoglobin SS disease	false	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Is a	Thalassemia with other hemoglobinopathy	true	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-thalassemia disease	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Causative agent	Hemoglobin S	false	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-thalassemia disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-thalassemia disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-thalassemia disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-thalassemia disease	Is a	Hereditary red blood cell disorder	false	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Is a	Disorder of hematopoietic structure	true	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Finding site	Erythroid cell	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-thalassemia disease	Is a	Sickling disorder due to hemoglobin S	true	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Associated morphology	Drepanocyte	true	Inferred relationship	Existential restriction modifier	1
Sickle cell-thalassemia disease	Finding site	Hematopoietic system structure	true	Inferred relationship	Existential restriction modifier	1
Sickle cell-thalassemia disease	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-thalassemia disease	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	3
Sickle cell-thalassemia disease	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-thalassemia disease	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	3
Sickle cell-thalassemia disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	4
Sickle cell-thalassemia disease	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	4
Sickle cell-thalassemia disease	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	3

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-beta-thalassemia	Is a	True	Sickle cell-thalassemia disease	Inferred relationship	Existential restriction modifier
Sickle cell-delta beta^0^-thalassemia	Is a	False	Sickle cell-thalassemia disease	Inferred relationship	Existential restriction modifier
Sickle cell anemia with coexistent alpha-thalassemia	Is a	True	Sickle cell-thalassemia disease	Inferred relationship	Existential restriction modifier
Sickle cell trait with coexistent alpha-thalassemia	Is a	False	Sickle cell-thalassemia disease	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease with crisis	Is a	True	Sickle cell-thalassemia disease	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease without crisis	Is a	True	Sickle cell-thalassemia disease	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
60878015	Hemoglobin S-F disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
60879011	Thalassemia-hemoglobin S disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
60880014	Sickle cell-thalassemia disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
60881013	Microdrepanocytic disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
60882018	Microdrepanocytosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
486462013	Sickle cell-thalassaemia disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
486463015	Haemoglobin S-F disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
486464014	Thalassaemia-haemoglobin S disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
768228015	Sickle cell-thalassemia disease (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3035990017	Sickle cell thalassaemia disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3036285019	Sickle cell thalassemia disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module