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23269001: Double heterozygous sickling disorder (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)\Double heterozygous sickling 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)\Double heterozygous sickling 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)\Double heterozygous sickling disorder

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

Descriptions:

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Sickle cell-beta-thalassaemia	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell-haemoglobin Lepore disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell-Hemoglobin O Arab disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell-hemoglobin D disease (disorder)	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell-hemoglobin C disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Sickle cell-hemoglobin E disease	Is a	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier (core metadata concept)
Glomerular disease due to double heterozygous sickling disorder	Due to	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Gouty arthropathy due to double heterozygous sickling disorder	Due to	True	Double heterozygous sickling disorder	Inferred relationship	Existential restriction modifier (core metadata concept)	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 (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
752769019	Double heterozygous sickling disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
39059017	Double heterozygous sickling disorder	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
39059017	Double heterozygous sickling disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
752769019	Double heterozygous sickling disorder (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
752769019	Double heterozygous sickling disorder (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6089781000241115	hémoglobinopathie double hétérozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6089791000241118	hémoglobinose double hétérozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6089781000241115	hémoglobinopathie double hétérozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6089791000241118	hémoglobinose double hétérozygote	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module