717811007: Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined immunodeficiency due to calcium release activated calcium channel dysfunction
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Combined immunodeficiency due to calcium release activated calcium channel dysfunction

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3323598012	Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3323599016	Combined immunodeficiency due to CRAC (calcium release activated calcium) channel dysfunction	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3323600018	Combined immunodeficiency due to CRAC channel dysfunction	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3323601019	Immune dysfunction with T-cell inactivation due to calcium entry defect	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3331180018	Combined immunodeficiency due to calcium release activated calcium channel dysfunction	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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