1197415001: Susceptibility to infection due to tyrosine kinase 2 deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Mendelian susceptibility to mycobacterial disease\Susceptibility to infection due to tyrosine kinase 2 deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Susceptibility to infection due to tyrosine kinase 2 deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Mendelian susceptibility to mycobacterial disease\Susceptibility to infection due to tyrosine kinase 2 deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4696251016	Autosomal recessive hyper-IgE (immunoglobulin E) syndrome due to TYK2 deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4696252011	Susceptibility to infection due to tyrosine kinase 2 deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4696253018	Susceptibility to infection due to TYK2 deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4696254012	Susceptibility to infection due to tyrosine kinase 2 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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