784340000: Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined immunodeficiency due to interleukin 21 receptor deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Combined immunodeficiency due to interleukin 21 receptor deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3763681013	Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3763682018	Combined immunodeficiency due to IL21R deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3763683011	Combined immunodeficiency due to interleukin 21 receptor deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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