417357006: Sickling disorder due to hemoglobin S (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

\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
\Red blood cell disorder\Hemoglobinopathy\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S

\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
\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
\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
\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
\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
\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
\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
\Disease\Congenital disease\Hereditary hemoglobinopathy\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S\Sickling disorder due to hemoglobin S

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2005. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

2546044010 Sickling disorder due to hemoglobin S (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

2548313018 Sickling disorder due to hemoglobin S en Synonym Active Only initial character case insensitive SNOMED CT core module

2548314012 Sickling disorder due to haemoglobin S en Synonym Active Only initial character case insensitive SNOMED CT core module

2553616013 Sickle cell disease en Synonym Active Entire term case insensitive SNOMED CT core module

2553617016 Sickle cell syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hemoglobin S sickling disorder with crisis	Is a	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier
Hemoglobin S sickling disorder without crisis	Is a	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier
Sickle cell-hemoglobin SS disease	Is a	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier
Double heterozygous sickling disorder	Is a	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier
Sickle cell-thalassemia disease	Is a	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier
Sickle cell nephropathy	Due to	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Hand-foot syndrome in sickle cell anemia	Due to	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Disorder of myocardium due to sickle cell hemoglobinopathy	Due to	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Suspected sickle cell disease	Associated finding	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Sickle cell disease not suspected	Associated finding	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Arthropathy due to sickle cell disease	Due to	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Priapism due to sickle cell disease	Due to	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Renal papillary necrosis due to sickle cell disease	Due to	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Focal segmental glomerulosclerosis due to sickle cell disease	Due to	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	1
Disorder of liver due to sickle cell disease	Due to	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier	2
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome	Is a	True	Sickling disorder due to hemoglobin S	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
2546044010	Sickling disorder due to hemoglobin S (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
2548313018	Sickling disorder due to hemoglobin S	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2548314012	Sickling disorder due to haemoglobin S	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2553616013	Sickle cell disease	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2553617016	Sickle cell syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module