445542007: Hemoglobin O-Arab trait (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 O-Arab trait

\Heterozygous haemoglobinopathy\Haemoglobin O-Arab trait

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin O-Arab trait
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Heterozygous haemoglobinopathy\Haemoglobin O-Arab trait
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Haemoglobin O-Arab trait
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Heterozygous haemoglobinopathy\Haemoglobin O-Arab trait

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

Status: current, Primitive. Date: 31-Jul 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2870553013 Hemoglobin O-Arab trait (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

2872029017 Hemoglobin O-Arab trait en Synonym Active Initial character case insensitive SNOMED CT core

2872030010 Haemoglobin O-Arab trait en Synonym Active Initial character case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Haemoglobin O-Arab trait	Is a	Heterozygous haemoglobinopathy	true	Inferred relationship	Some
Haemoglobin O-Arab trait	Is a	Hereditary haemoglobinopathy due to globin chain mutation	true	Inferred relationship	Some
Haemoglobin O-Arab trait	Finding site	Body system structure	false	Inferred relationship	Some
Haemoglobin O-Arab trait	Finding site	Erythrocyte	false	Inferred relationship	Some
Haemoglobin O-Arab trait	Occurrence	Congenital	true	Inferred relationship	Some	1
Haemoglobin O-Arab trait	Finding site	Erythrocyte	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2870553013	Hemoglobin O-Arab trait (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2872029017	Hemoglobin O-Arab trait	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2872030010	Haemoglobin O-Arab trait	en	Synonym	Active	Initial character case insensitive	SNOMED CT core