1186714005: Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary cancer-predisposing syndrome\Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency
• \Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency
• \Disorder of hematopoietic cell proliferation\Lymphoproliferative disorder\Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4667409013	Combined immunodeficiency due to IL2 inducible T cell kinase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4667411016	Combined immunodeficiency due to ITK deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4667412011	Autosomal recessive lymphoproliferative disease due to ITK deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4667656019	Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
4667657011	Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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