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25065001: Hemoglobin E disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of blood, lymphatics and immune system\Blood disease\...

\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease
\Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin E disease

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

41996013 Hemoglobin E disease en Synonym Active Case sensitive SNOMED CT core

41997016 Hemoglobin E-E disease en Synonym Active Case sensitive SNOMED CT core

482564013 Haemoglobin E-E disease en Synonym Active Case sensitive SNOMED CT core

482565014 Haemoglobin E disease en Synonym Active Case sensitive SNOMED CT core

482566010 Homozygous for Hb E en Synonym Active Initial character case insensitive SNOMED CT core

755202015 Hemoglobin E disease (disorder) en Fully specified name Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Haemoglobin E disease	Is a	Hereditary haemoglobinopathy due to globin chain mutation	true	Inferred relationship	Some
Haemoglobin E disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Haemoglobin E disease	Finding site	Body system structure	false	Inferred relationship	Some
Haemoglobin E disease	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Some
Haemoglobin E disease	Occurrence	Congenital	true	Inferred relationship	Some	1
Haemoglobin E disease	Finding site	Erythrocyte	true	Inferred relationship	Some	1
Haemoglobin E disease	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Haemoglobin E disease	Finding site	Erythrocyte	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Haemoglobin E/beta thalassaemia disease	Is a	True	Haemoglobin E disease	Inferred relationship	Some
Family history of haemoglobinopathy E	Associated finding	True	Haemoglobin E disease	Inferred relationship	Some	1

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
41996013	Hemoglobin E disease	en	Synonym	Active	Case sensitive	SNOMED CT core
41997016	Hemoglobin E-E disease	en	Synonym	Active	Case sensitive	SNOMED CT core
482564013	Haemoglobin E-E disease	en	Synonym	Active	Case sensitive	SNOMED CT core
482565014	Haemoglobin E disease	en	Synonym	Active	Case sensitive	SNOMED CT core
482566010	Homozygous for Hb E	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
755202015	Hemoglobin E disease (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core