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36472007: Sickle cell-thalassemia disease (disorder)

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

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood (disorder)\...

\Hereditary disorder of cellular element of blood (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

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

\Procedure related finding\Evaluation finding\...

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (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
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Disease\Disorder of foetus and/or newborn\Congenital disease (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
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (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
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Disease\Disorder of cellular component of blood (disorder)\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Disease\Disorder of cellular component of blood (disorder)\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
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\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
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Sickle cell-thalassemia disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (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
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\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
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\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
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Thalassemia with other hemoglobinopathy\Sickle cell-thalassemia disease

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

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

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 (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
60879011	Thalassemia-hemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
60880014	Sickle cell-thalassemia disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
60881013	Microdrepanocytic disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
60882018	Microdrepanocytosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
486462013	Sickle cell-thalassaemia disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
486463015	Haemoglobin S-F disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
486464014	Thalassaemia-haemoglobin S disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
768228015	Sickle cell-thalassemia disease (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3035990017	Sickle cell thalassaemia disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3036285019	Sickle cell thalassemia disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core