766983005: Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Susceptibility to respiratory infection associated with CD8alpha chain mutation
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Susceptibility to respiratory infection associated with CD8alpha chain mutation

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3663569017	Familial CD8 deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3663570016	Susceptibility to respiratory infection associated with CD8alpha chain mutation	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3663571017	Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3663572012	A rare primary immunodeficiency due to a defect in adaptive immunity characterised by the absence of CD8 positive T cells with normal immunoglobulin and specific antibody titres in blood and susceptibility to recurrent respiratory bacterial and viral infections. Symptom severity ranges from fatal respiratory insufficiency to mild or asymptomatic phenotypes.	en	Definition	Active	Case sensitive	SNOMED CT core
3663573019	A rare primary immunodeficiency due to a defect in adaptive immunity characterized by the absence of CD8 positive T cells with normal immunoglobulin and specific antibody titers in blood and susceptibility to recurrent respiratory bacterial and viral infections. Symptom severity ranges from fatal respiratory insufficiency to mild or asymptomatic phenotypes.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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