417357006: Sickling disorder due to hemoglobin S (disorder)

SNOMED CT Concept\Clinical finding (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 (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)

\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)
\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)
\Disease\Disorder of cellular component of blood\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of cellular element of blood\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Hereditary red blood cell disorder (disorder)\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)
\Disease\Disorder of body system\Red blood cell disorder\Haemoglobinopathy\Hereditary hemoglobinopathy (disorder)\Hereditary hemoglobinopathy due to globin chain mutation\Hereditary hemoglobin S (disorder)\Sickling disorder due to hemoglobin S (disorder)

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

Descriptions:

Expanded Value Set

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

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

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 (core metadata concept)	SNOMED CT core
2548313018	Sickling disorder due to hemoglobin S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2548314012	Sickling disorder due to haemoglobin S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2553616013	Sickle cell disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2553617016	Sickle cell syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2546044010	Sickling disorder due to hemoglobin S (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2548313018	Sickling disorder due to hemoglobin S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2548314012	Sickling disorder due to haemoglobin S	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2553616013	Sickle cell disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2553616013	Sickle cell disease	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2553617016	Sickle cell syndrome	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2553617016	Sickle cell syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
955281000195114	disturbo falciforme da emoglobina S	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5283521000241116	affection drépanocytaire due à l'hémoglobine S	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5283521000241116	affection drépanocytaire due à l'hémoglobine S	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
955281000195114	disturbo falciforme da emoglobina S	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module