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Results 1 - 10 of 96 for "T-cell" immunodeficiency
  1. T-cell immunodeficiency, congenital alopecia, and nail dystrophy 
    T-cell immunodeficiency, congenital alopecia, and nail dystrophy is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized ...
    https://medlineplus.gov/...cy-congenital-alopecia-and-nail-dystrophy - Genetics
  2. FOXN1 gene 
    ... the FOXN1 gene has been found to cause T-cell immunodeficiency, congenital alopecia, and nail dystrophy, a condition that ... to fight infections. As a result, people with T-cell immunodeficiency, congenital alopecia, and nail dystrophy develop recurrent serious ...
    https://medlineplus.gov/genetics/gene/foxn1 - Genetics
  3. ZAP70-related severe combined immunodeficiency 
    ... No abstract available. Citation on PubMed Elder ME. T-cell immunodeficiencies. Pediatr Clin North Am. 2000 Dec;47(6): ... PubMed Grunebaum E, Sharfe N, Roifman CM. Human T cell immunodeficiency: when signal transduction goes wrong. Immunol Res. 2006; ...
    https://medlineplus.gov/...-related-severe-combined-immunodeficiency - Genetics
  4. ZAP70 gene 
    ... No abstract available. Citation on PubMed Elder ME. T-cell immunodeficiencies. Pediatr Clin North Am. 2000 Dec;47(6): ... PubMed Grunebaum E, Sharfe N, Roifman CM. Human T cell immunodeficiency: when signal transduction goes wrong. Immunol Res. 2006; ...
    https://medlineplus.gov/genetics/gene/zap70 - Genetics
  5. MAGT1 gene 
    ... Second messenger role for Mg2+ revealed by human T-cell immunodeficiency. Nature. 2011 Jul 27;475(7357):471-6. ... of MAGT1 abrogates the Mg2+ flux required for T cell signaling and leads to a novel human primary immunodeficiency. Magnes Res. 2011 Sep;24(3):S109-14. ...
    https://medlineplus.gov/genetics/gene/magt1 - Genetics
  6. X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia 
    ... Second messenger role for Mg2+ revealed by human T-cell immunodeficiency. Nature. 2011 Jul 27;475(7357):471-6. ... of MAGT1 abrogates the Mg2+ flux required for T cell signaling and leads to a novel human primary immunodeficiency. Magnes Res. 2011 Sep;24(3):S109-14. ...
    https://medlineplus.gov/...pstein-barr-virus-infection-and-neoplasia - Genetics
  7. Immune System and Disorders (National Library of Medicine)  
    What is the immune system? Your immune system is a complex network of cells, tissues, and organs. Together they help the body fight infections and other ...
    https://medlineplus.gov/immunesystemanddisorders.html - Health Topics
  8. NFKBIA gene 
    ... associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency. J Clin Invest. 2003 Oct;112(7):1108- ...
    https://medlineplus.gov/genetics/gene/nfkbia - Genetics
  9. Activated PI3K-delta syndrome 
    ... 14 Immunodeficiency 36 P110δ-activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency PASLI Genetic Testing Registry: Immunodeficiency 14 Genetic Testing ...
    https://medlineplus.gov/.../condition/activated-pi3k-delta-syndrome - Genetics
  10. Adenosine deaminase deficiency 
    ... combined immunodeficiency due to ADA deficiency Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due ...
    https://medlineplus.gov/.../condition/adenosine-deaminase-deficiency - Genetics
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