127046009: Sickle cell trait with coexistent alpha-thalassemia (disorder)

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

\Evaluation finding\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\Evaluation finding\Hematopoietic system finding\Hemoglobin level outside reference range (finding)\Hemoglobin low\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia

\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)\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\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)\Heterozygous hemoglobinopathy\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\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\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\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)\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\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)\Heterozygous hemoglobinopathy\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\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\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of cellular component of blood (disorder)\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\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)\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\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)\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\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)\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\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)\Heterozygous hemoglobinopathy\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\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\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\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)\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy\Sickle cell trait\Sickle cell trait with coexistent alpha-thalassemia
\Disease\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Alpha thalassemia (disorder)\Sickle cell trait with coexistent alpha-thalassemia

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 trait with coexistent alpha-thalassemia	Is a	Sickle cell-thalassemia disease	false	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassemia	Is a	Sickle cell trait	true	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassemia	Causative agent	Hemoglobin S	false	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassemia	Associated morphology	Drepanocyte	false	Inferred relationship	Some	1
Sickle cell trait with coexistent alpha-thalassemia	Finding site	Erythrocyte	false	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassemia	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some	1
Sickle cell trait with coexistent alpha-thalassemia	Has definitional manifestation	erytropeni	false	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Some	2
Sickle cell trait with coexistent alpha-thalassemia	Associated morphology	Drepanocyte	false	Inferred relationship	Some	1
Sickle cell trait with coexistent alpha-thalassemia	Associated morphology	Drepanocyte	false	Inferred relationship	Some	2
Sickle cell trait with coexistent alpha-thalassemia	Finding site	Erythroid cell (cell)	false	Inferred relationship	Some	1
Sickle cell trait with coexistent alpha-thalassemia	Is a	Alpha thalassemia (disorder)	true	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassemia	Finding site	Body system structure	false	Inferred relationship	Some
Sickle cell trait with coexistent alpha-thalassemia	Has interpretation	Below reference range	false	Inferred relationship	Some	1
Sickle cell trait with coexistent alpha-thalassemia	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
Sickle cell trait with coexistent alpha-thalassemia	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Sickle cell trait with coexistent alpha-thalassemia	Interprets	Red blood cell count	false	Inferred relationship	Some	2
Sickle cell trait with coexistent alpha-thalassemia	Occurrence	Congenital	true	Inferred relationship	Some	3
Sickle cell trait with coexistent alpha-thalassemia	Finding site	Erythrocyte	true	Inferred relationship	Some	3
Sickle cell trait with coexistent alpha-thalassemia	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
334019	Sickle cell trait with coexistent alpha-thalassemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
474039012	Sickle cell trait with coexistent alpha-thalassaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
731085011	Sickle cell trait with coexistent alpha-thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3330291000052118	heterozygot för hemoglobin S, med samtidig alfatalassemi	sv	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)