934007: Thalassemia intermedia (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 intermedia
\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 intermedia
\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 intermedia
\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 intermedia
\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 intermedia

\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 intermedia

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

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

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

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

2644018 Thalassemia intermedia en Synonym Active Entire term case insensitive SNOMED CT core module

510307010 Thalassaemia intermedia en Synonym Active Entire term case insensitive SNOMED CT core module

837127011 Thalassemia intermedia (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 intermedia	Is a	Thalassemia	true	Inferred relationship	Existential restriction modifier
Thalassemia intermedia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Thalassemia intermedia	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Thalassemia intermedia	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Thalassemia intermedia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Thalassemia intermedia	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Thalassemia intermedia	Has interpretation	Below reference range	false	Inferred relationship	Existential restriction modifier	1
Thalassemia intermedia	Interprets	Measurement of total hemoglobin concentration	false	Inferred relationship	Existential restriction modifier	1
Thalassemia intermedia	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	2
Thalassemia intermedia	Interprets	Red blood cell count	false	Inferred relationship	Existential restriction modifier	2
Thalassemia intermedia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Thalassemia intermedia	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	3
Thalassemia intermedia	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
2644018	Thalassemia intermedia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
510307010	Thalassaemia intermedia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
837127011	Thalassemia intermedia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module