119691000119106: Hemoglobin C/beta 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\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)

\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)

\Procedure related finding\Evaluation finding\...

\Measurement finding\Finding of substance level (finding)\Protein level - finding\Hemoglobin finding\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range (finding)\Hemoglobin below reference range (finding)\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)

\Hematopoietic system finding\Haematology test outside reference range\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range (finding)\Hemoglobin below reference range (finding)\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)

\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\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\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\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\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\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\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\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of cellular component of blood (disorder)\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\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\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of cellular component of blood (disorder)\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\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\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\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\Beta thalassemia\Hemoglobin C/beta thalassemia disease (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\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin C disease\Hemoglobin C/beta thalassemia disease (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Thalassemia\Beta thalassemia\Hemoglobin C/beta thalassemia disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2017. Module: US National Library of Medicine maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

747361000124119 Hemoglobin C/beta thalassemia disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)

747371000124114 Hemoglobin C/beta thalassemia disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) US National Library of Medicine maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemoglobin C/beta thalassemia disease (disorder)	Is a	Hemoglobin C disease	true	Inferred relationship	Some
Hemoglobin C/beta thalassemia disease (disorder)	Is a	Beta thalassemia	true	Inferred relationship	Some
Hemoglobin C/beta thalassemia disease (disorder)	Finding site	Erythrocyte	false	Inferred relationship	Some
Hemoglobin C/beta thalassemia disease (disorder)	Has interpretation	Below reference range	false	Inferred relationship	Some	1
Hemoglobin C/beta thalassemia disease (disorder)	Interprets	Red blood cell count	false	Inferred relationship	Some	1
Hemoglobin C/beta thalassemia disease (disorder)	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Hemoglobin C/beta thalassemia disease (disorder)	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2
Hemoglobin C/beta thalassemia disease (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	3
Hemoglobin C/beta thalassemia disease (disorder)	Finding site	Erythrocyte	true	Inferred relationship	Some	3

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
747361000124119	Hemoglobin C/beta thalassemia disease (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	US National Library of Medicine maintained module (core metadata concept)
747371000124114	Hemoglobin C/beta thalassemia disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	US National Library of Medicine maintained module (core metadata concept)