35434009: Sickle cell-hemoglobin C 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 C 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 C 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 C disease
• \Red blood cell disorder\Haemoglobinopathy\Mixed haemoglobin disorder\Sickle cell-haemoglobin C 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 C 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 C 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 C 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 C disease
• \Disease\Blood disease\Red blood cell disorder\Haemoglobinopathy\Mixed haemoglobin disorder\Sickle cell-haemoglobin C 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 C 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 C 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 C disease
• \Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Mixed haemoglobin disorder\Sickle cell-haemoglobin C 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 C disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
197149012	Hb SC disease	en	Synonym	Active	Case sensitive	SNOMED CT core
3036098017	Sickle cell hemoglobin C	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3036334012	Sickle cell haemoglobin C	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
486158014	Double heterozygous for Hb S and Hb D	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
486159018	Sickle cell-haemoglobin C disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
486160011	Sickle cell anaemia with haemoglobin C disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
486161010	Haemoglobin S/C disease	en	Synonym	Active	Case sensitive	SNOMED CT core
486162015	Hemoglobin S/C disease	en	Synonym	Active	Case sensitive	SNOMED CT core
486163013	Sickle cell anemia with hemoglobin C disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
486164019	Haemoglobin S-C disease	en	Synonym	Active	Case sensitive	SNOMED CT core
59117010	Sickle cell-hemoglobin C disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
59118017	Hemoglobin S-C disease	en	Synonym	Active	Case sensitive	SNOMED CT core
59119013	HbS-HbC disease	en	Synonym	Active	Case sensitive	SNOMED CT core
767073016	Sickle cell-hemoglobin C disease (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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