Immunoglobulin Kappa Light Chain Deficiency (IGKCD)

Alias:
Recurrent Infections Associated with Rare Immunoglobulin Isotypes Deficiency
Kappa Light Chain Deficiency
Kappa Chain Deficiency
Kappa-Chain Deficiency
Igkcd
Igg Subclass Deficiency with Iga Subclass Deficiency
Selective Igg Subclass Deficiency
Isolated Igg Subclass Deficiency
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Immunoglobulin Kappa Light Chain Deficiency, also known as recurrent infections associated with rare immunoglobulin isotypes deficiency, is related to hyper-ige syndrome 1, autosomal dominant, with recurrent infections and systemic lupus erythematosus. An important gene associated with Immunoglobulin Kappa Light Chain Deficiency is IGKC (Immunoglobulin Kappa Constant), and among its related pathways/superpathways are Development Angiotensin activation of ERK and Immune response NFAT in immune response. Affiliated tissues include liver and skin, and related phenotypes are recurrent respiratory infections and recurrent upper respiratory tract infections
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
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Reference
MALACARDS
AR
Child
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4

Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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