127048005: Sickle cell-Hemoglobin O Arab disease (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\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease

\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\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease
\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\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease
\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\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease
\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\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S\Double heterozygous sickling disorder\Sickle cell-Hemoglobin O Arab disease

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

336017 Sickle cell-Hemoglobin O Arab disease en Synonym Active Only initial character case insensitive SNOMED CT core module
474041013 Sickle cell-Haemoglobin O Arab disease en Synonym Active Only initial character case insensitive SNOMED CT core module
731087015 Sickle cell-Hemoglobin O Arab disease (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sickle cell-Hemoglobin O Arab disease	Is a	Sickle cell-hemoglobin SS disease	false	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Causative agent	Hemoglobin S	false	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-Hemoglobin O Arab disease	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-Hemoglobin O Arab disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-Hemoglobin O Arab disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-Hemoglobin O Arab disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-Hemoglobin O Arab disease	Is a	Disorder of hematopoietic structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Finding site	Erythroid cell	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-Hemoglobin O Arab disease	Is a	Double heterozygous sickling disorder	true	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Sickle cell-Hemoglobin O Arab disease	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 sickle cell-haemoglobin O Arab disease (situation)	Associated finding	True	Sickle cell-Hemoglobin O Arab disease	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
336017	Sickle cell-Hemoglobin O Arab disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
474041013	Sickle cell-Haemoglobin O Arab disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
731087015	Sickle cell-Hemoglobin O Arab disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module