47047009: Thalassemia with other hemoglobinopathy (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)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)

\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (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\Thalassemia with other hemoglobinopathy (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\Thalassemia with other hemoglobinopathy (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\Thalassemia with other hemoglobinopathy (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\Thalassemia with other hemoglobinopathy (disorder)
\Haematopoietic system finding\Haemoglobin finding\Haemoglobin level outside reference range\Hemoglobin below reference range (finding)\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassemia with other hemoglobinopathy (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\Thalassemia with other hemoglobinopathy (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (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\Thalassemia with other hemoglobinopathy (disorder)
\Disease\Disorder of cellular component of blood\Anaemia\Anaemia due to disturbance of haemoglobin synthesis\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (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\Thalassemia with other hemoglobinopathy (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassaemia\Thalassemia with other hemoglobinopathy (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
Thalassemia with other hemoglobinopathy (disorder)	Is a	Thalassaemia	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia with other hemoglobinopathy (disorder)	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia with other hemoglobinopathy (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia with other hemoglobinopathy (disorder)	Has definitional manifestation	érythropénie	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia with other hemoglobinopathy (disorder)	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia with other hemoglobinopathy (disorder)	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia with other hemoglobinopathy (disorder)	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Thalassemia with other hemoglobinopathy (disorder)	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Thalassemia with other hemoglobinopathy (disorder)	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Thalassemia with other hemoglobinopathy (disorder)	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Thalassemia with other hemoglobinopathy (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Thalassemia with other hemoglobinopathy (disorder)	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Thalassemia with other hemoglobinopathy (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
Sickle cell-thalassemia disease	Is a	True	Thalassemia with other hemoglobinopathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease	Is a	True	Thalassemia with other hemoglobinopathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemoglobin D beta plus thalassaemia	Is a	True	Thalassemia with other hemoglobinopathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemoglobin E beta plus thalassaemia	Is a	True	Thalassemia with other hemoglobinopathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Haemoglobin C beta plus thalassaemia	Is a	True	Thalassemia with other hemoglobinopathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hemoglobin E beta zero thalassemia (disorder)	Is a	True	Thalassemia with other hemoglobinopathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hemoglobin D beta zero thalassemia (disorder)	Is a	True	Thalassemia with other hemoglobinopathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Hemoglobin C beta zero thalassemia (disorder)	Is a	True	Thalassemia with other hemoglobinopathy (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
78417011	Thalassemia with other hemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
494734018	Thalassaemia with other haemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
784462017	Thalassemia with other hemoglobinopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
78417011	Thalassemia with other hemoglobinopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
78417011	Thalassemia with other hemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
494734018	Thalassaemia with other haemoglobinopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
494734018	Thalassaemia with other haemoglobinopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
784462017	Thalassemia with other hemoglobinopathy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
784462017	Thalassemia with other hemoglobinopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4543551000241117	thalassémie avec hémoglobinopathie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4543551000241117	thalassémie avec hémoglobinopathie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module