234392002: Hemoglobin E/beta thalassemia disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\Finding of substance level\Finding of protein level\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Evaluation finding\Measurement finding\Measurement finding outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Evaluation finding\Hematopoietic system finding\Hematology test outside reference range\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease

\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\Hereditary hemoglobinopathy\...

\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease

\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease

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

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin E disease\Hemoglobin E/beta thalassemia disease
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Hemoglobin E/beta thalassemia disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

351167019 Hemoglobin E/beta thalassemia disease en Synonym Active Only initial character case insensitive SNOMED CT core module

351168012 Double heterozygous for Hb E and beta thalassaemia en Synonym Active Only initial character case insensitive SNOMED CT core module

351169016 Haemoglobin E/beta thalassaemia disease en Synonym Active Only initial character case insensitive SNOMED CT core module

351170015 Double heterozygous for Hb E and beta thalassemia en Synonym Active Only initial character case insensitive SNOMED CT core module

622704011 Hemoglobin E/beta thalassemia disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hemoglobin E/beta thalassemia disease	Is a	Hemoglobin E disease	true	Inferred relationship	Existential restriction modifier
Hemoglobin E/beta thalassemia disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hemoglobin E/beta thalassemia disease	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Hemoglobin E/beta thalassemia disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Hemoglobin E/beta thalassemia disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Hemoglobin E/beta thalassemia disease	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Existential restriction modifier
Hemoglobin E/beta thalassemia disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Hemoglobin E/beta thalassemia disease	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	1
Hemoglobin E/beta thalassemia disease	Is a	Beta thalassemia	true	Inferred relationship	Existential restriction modifier
Hemoglobin E/beta thalassemia disease	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Hemoglobin E/beta thalassemia disease	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	2
Hemoglobin E/beta thalassemia disease	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-delta beta^0^-thalassemia	Is a	False	Hemoglobin E/beta thalassemia disease	Inferred relationship	Existential restriction modifier
Haemoglobin E beta zero thalassaemia (disorder)	Is a	True	Hemoglobin E/beta thalassemia disease	Inferred relationship	Existential restriction modifier
Haemoglobin E beta plus thalassaemia (disorder)	Is a	True	Hemoglobin E/beta thalassemia disease	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
351167019	Hemoglobin E/beta thalassemia disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
351168012	Double heterozygous for Hb E and beta thalassaemia	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
351169016	Haemoglobin E/beta thalassaemia disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
351170015	Double heterozygous for Hb E and beta thalassemia	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
622704011	Hemoglobin E/beta thalassemia disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module