23269001: Double heterozygous sickling disorder (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

\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
\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

\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
\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
\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
\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
\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
\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
\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
\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

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

39059017 Double heterozygous sickling disorder en Synonym Active Entire term case insensitive SNOMED CT core module

752769019 Double heterozygous sickling disorder (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Double heterozygous sickling disorder	Is a	Hemoglobinopathy	false	Inferred relationship	Existential restriction modifier
Double heterozygous sickling disorder	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Double heterozygous sickling disorder	Finding site	Erythrocyte	false	Inferred relationship	Existential restriction modifier
Double heterozygous sickling disorder	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier
Double heterozygous sickling disorder	Has definitional manifestation	Red blood cell finding	false	Inferred relationship	Existential restriction modifier
Double heterozygous sickling disorder	Is a	Sickling disorder due to hemoglobin S	true	Inferred relationship	Existential restriction modifier
Double heterozygous sickling disorder	Finding site	Body system structure	false	Inferred relationship	Existential restriction modifier
Double heterozygous sickling disorder	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Double heterozygous sickling disorder	Finding site	Erythrocyte	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-beta-thalassemia	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin Lepore disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier
Sickle cell-Hemoglobin O Arab disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin D disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin C disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin E disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier
Disorder of glomerulus due to double heterozygous sickling disorder	Due to	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier	2
Gouty arthropathy due to double heterozygous sickling disorder	Due to	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier	3

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
39059017	Double heterozygous sickling disorder	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
752769019	Double heterozygous sickling disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module