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

SNOMED CT Concept\Clinical finding (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 (disorder)\Hereditary hemoglobinopathy (disorder)\...

\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)

\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)

\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (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 (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)

\Procedure related finding\Evaluation finding\...

\Measurement finding\Finding of substance level (finding)\Finding of protein level (finding)\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Measurement finding\Measurement finding outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)

\Haematopoietic system finding\Haematology test outside reference range\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\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 (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\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 (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Heterozygous hemoglobinopathy (disorder)\Sickle cell trait (disorder)\Sickle cell trait with coexistent alpha-thalassemia (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Alpha thalassemia\Sickle cell trait with coexistent alpha-thalassemia (disorder)

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

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
334019	Sickle cell trait with coexistent alpha-thalassemia	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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