445542007: Hemoglobin O-Arab trait (disorder)

SNOMED CT Concept\Clinical finding\...

\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\...

\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait

\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait
\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin 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 hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin 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 hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin 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 hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin 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 hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hemoglobin O-Arab trait
\Disease\Congenital disease\Hereditary hemoglobinopathy\Heterozygous hemoglobinopathy\Hemoglobin O-Arab trait

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2010. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

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

2872029017 Hemoglobin O-Arab trait en Synonym Active Only initial character case insensitive SNOMED CT core module

2872030010 Haemoglobin O-Arab trait en Synonym Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with Haemoglobin O-Arab carrier (situation)	Associated finding	True	Hemoglobin O-Arab trait	Inferred relationship	Existential restriction modifier	1
Result consistent with haemoglobin O-Arab carrier	Associated finding	True	Hemoglobin O-Arab trait	Inferred relationship	Existential restriction modifier	1

This concept is not in any reference sets

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