26682008: Homozygous beta thalassemia (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\Homozygous beta thalassemia
\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\Homozygous beta thalassemia
\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\Homozygous beta thalassemia
\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\Homozygous beta thalassemia
\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\Homozygous beta thalassemia

\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\Thalassemia\Beta thalassemia\Homozygous beta thalassemia

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Homozygous beta thalassemia

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Homozygous beta thalassemia
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Homozygous beta thalassemia

\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\Homozygous beta thalassemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Homozygous beta thalassemia
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Beta thalassemia\Homozygous beta thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Homozygous beta thalassemia
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Homozygous beta thalassemia
\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\Homozygous beta thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Homozygous beta thalassemia
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Homozygous beta thalassemia
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Beta thalassemia\Homozygous beta thalassemia

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

44671012 Homozygous beta thalassemia en Synonym Active Entire term case insensitive SNOMED CT core module

44672017 Cooley's anemia en Synonym Active Entire term case sensitive SNOMED CT core module

44673010 Mediterranean anemia en Synonym Active Entire term case sensitive SNOMED CT core module

483318012 Beta thalassaemia major en Synonym Active Entire term case insensitive SNOMED CT core module

483319016 Cooley's anaemia en Synonym Active Entire term case sensitive SNOMED CT core module

483320010 Homozygous beta thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module

757162012 Homozygous beta thalassemia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Homozygous beta thalassemia	Is a	Beta thalassemia	true	Inferred relationship	Existential restriction modifier
Homozygous beta thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Homozygous beta thalassemia	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Homozygous beta thalassemia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Homozygous beta thalassemia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Homozygous beta thalassemia	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Homozygous beta thalassemia	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Homozygous beta thalassemia	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Homozygous beta thalassemia	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Homozygous beta thalassemia	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	2
Homozygous beta thalassemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Homozygous beta thalassemia	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Homozygous beta thalassemia	Interprets	Measurement of total hemoglobin concentration	true	Inferred relationship	Existential restriction modifier	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
44671012	Homozygous beta thalassemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
44672017	Cooley's anemia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
44673010	Mediterranean anemia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
483318012	Beta thalassaemia major	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
483319016	Cooley's anaemia	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
483320010	Homozygous beta thalassaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
757162012	Homozygous beta thalassemia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module