75451007: Thalassemia major (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\Thalassemia major
\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\Thalassemia major
\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\Thalassemia major
\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\Thalassemia major
\Evaluation finding\Hematopoietic system finding\Hemoglobin finding\Hemoglobin level outside reference range\Hemoglobin below reference range\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia major

\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\Thalassemia major

\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia major

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major
\Disease\Disorder of cellular component of blood\Anemia\Anemia due to disturbance of hemoglobin synthesis\Thalassemia\Thalassemia major
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major
\Disease\Congenital disease\Hereditary hemoglobinopathy\Thalassemia\Thalassemia major

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

125319013 Thalassemia major en Synonym Active Entire term case insensitive SNOMED CT core module

125322010 Homozygous thalassemia en Synonym Active Entire term case insensitive SNOMED CT core module

503017017 Thalassaemia major en Synonym Active Entire term case insensitive SNOMED CT core module

503018010 Homozygous thalassaemia en Synonym Active Entire term case insensitive SNOMED CT core module

816062015 Thalassemia major (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
Thalassemia major	Is a	Thalassemia	true	Inferred relationship	Existential restriction modifier
Thalassemia major	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Thalassemia major	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Thalassemia major	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Thalassemia major	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Thalassemia major	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Thalassemia major	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Thalassemia major	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Thalassemia major	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Thalassemia major	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	2
Thalassemia major	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Thalassemia major	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Thalassemia major	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
125319013	Thalassemia major	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
125322010	Homozygous thalassemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
503017017	Thalassaemia major	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
503018010	Homozygous thalassaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
816062015	Thalassemia major (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module