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

\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin O Arab disease
\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin 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 haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin O Arab 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\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin O Arab disease
\Disease\Blood disease\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin O Arab disease
\Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin 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 haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin O Arab disease
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin O Arab disease
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin O Arab disease
\Disease\Congenital disease\Hereditary haemoglobinopathy\Hereditary haemoglobinopathy due to globin chain mutation\Hereditary haemoglobin S\Sickling disorder due to haemoglobin S\Double heterozygous sickling disorder\Sickle cell-Haemoglobin O Arab disease

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

Descriptions:

Id Description Lang Type Status Case? Module

336017 Sickle cell-Hemoglobin O Arab disease en Synonym Active Initial character case insensitive SNOMED CT core

474041013 Sickle cell-Haemoglobin O Arab disease en Synonym Active Initial character case insensitive SNOMED CT core

731087015 Sickle cell-Hemoglobin O Arab disease (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core

Expanded Value Set

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