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934007: Thalassemia intermedia (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)\Thalassemia\Thalassemia intermedia

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

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

\Procedure related finding\Evaluation finding\...

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

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Thalassemia intermedia	Is a	Thalassemia	true	Inferred relationship	Some
Thalassemia intermedia	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Thalassemia intermedia	Finding site	Erythrocyte	false	Inferred relationship	Some
Thalassemia intermedia	Finding site	Hematopoietic system structure	false	Inferred relationship	Some
Thalassemia intermedia	Has definitional manifestation	Erythropenia	false	Inferred relationship	Some
Thalassemia intermedia	Finding site	Body system structure	false	Inferred relationship	Some
Thalassemia intermedia	Has interpretation	Below reference range	false	Inferred relationship	Some	1
Thalassemia intermedia	Interprets	Measurement of total haemoglobin concentration	false	Inferred relationship	Some	1
Thalassemia intermedia	Has interpretation	Below reference range	true	Inferred relationship	Some	2
Thalassemia intermedia	Interprets	Red blood cell count	false	Inferred relationship	Some	2
Thalassemia intermedia	Occurrence	Congenital	true	Inferred relationship	Some	3
Thalassemia intermedia	Finding site	Erythrocyte	true	Inferred relationship	Some	3
Thalassemia intermedia	Interprets	Measurement of total haemoglobin concentration	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Belgian GP subset (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2644018	Thalassemia intermedia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2645017	Thalassemia intermedia, NOS	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
510307010	Thalassaemia intermedia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
837127011	Thalassemia intermedia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1887491000172114	thalassémie intermédiaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
1887501000172116	intermedia thalassemie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)