1197478005: Primary immunodeficiency with multifaceted aberrant lymphoid immunity (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Primary immunodeficiency with multifaceted aberrant lymphoid immunity
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Primary immunodeficiency with multifaceted aberrant lymphoid immunity

Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4696499019	Primary immunodeficiency with multifaceted aberrant lymphoid immunity	en	Synonym	Active	Case insensitive	SNOMED CT core
4696500011	NIK deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
4696501010	NF-kappa-B-inducing kinase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
4696502015	Primary immunodeficiency with multifaceted aberrant lymphoid immunity (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4696503013	A rare genetic primary combined T and B cell immunodeficiency with characteristics of recurrent, severe viral and bacterial infections. Immunologic findings include decreased immunoglobulin levels, decreased numbers of B and NK cells, reduced relative CD19+ B cells in peripheral blood, impaired memory responses to viral infections and defective antigen-specific T-cell proliferation.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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