35434009: Sickle cell-hemoglobin C 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 C 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 C 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 C disease
\Red blood cell disorder\Hemoglobinopathy\Mixed hemoglobin disorder\Sickle cell-hemoglobin C 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 C 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 C 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 C 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 C disease
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hemoglobinopathy\Mixed hemoglobin disorder\Sickle cell-hemoglobin C 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 C 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 C 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 C disease
\Disease\Disorder of body system\Red blood cell disorder\Hemoglobinopathy\Mixed hemoglobin disorder\Sickle cell-hemoglobin C 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 C disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Sickle cell-hemoglobin C disease	Is a	Sickle cell-hemoglobin SS disease	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Is a	Mixed hemoglobin disorder	true	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin C disease	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin C disease	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Causative agent	Hemoglobin S	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin C disease	Has definitional manifestation	Erythropenia	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin C disease	Associated morphology	Drepanocyte	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-hemoglobin C disease	Is a	Disorder of hematopoietic structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Finding site	Erythroid cell	false	Inferred relationship	Existential restriction modifier	2
Sickle cell-hemoglobin C disease	Is a	Double heterozygous sickling disorder	true	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Sickle cell-hemoglobin C disease	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-hemoglobin C disease without crisis	Is a	True	Sickle cell-hemoglobin C disease	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease with crisis	Is a	True	Sickle cell-hemoglobin C disease	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C retinopathy	Due to	True	Sickle cell-hemoglobin C disease	Inferred relationship	Existential restriction modifier	2
National Health Service Sickle Cell and Thalassaemia Screening Programme result consistent with sickle cell-haemoglobin C disease (situation)	Associated finding	True	Sickle cell-hemoglobin C 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
59117010	Sickle cell-hemoglobin C disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
59118017	Hemoglobin S-C disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
59119013	HbS-HbC disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
197149012	Hb SC disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
486158014	Double heterozygous for Hb S and Hb D	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
486159018	Sickle cell-haemoglobin C disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
486160011	Sickle cell anaemia with haemoglobin C disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
486161010	Haemoglobin S/C disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
486162015	Hemoglobin S/C disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
486163013	Sickle cell anemia with hemoglobin C disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
486164019	Haemoglobin S-C disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
767073016	Sickle cell-hemoglobin C disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3036098017	Sickle cell hemoglobin C	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3036334012	Sickle cell haemoglobin C	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module