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Results 1 - 10 of 16 for Immunodeficiency 14
  1. Activated PI3K-delta syndrome 
    ... cell is sufficient to cause the disorder. APDS Immunodeficiency 14 Immunodeficiency 36 P110δ-activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency PASLI Genetic Testing Registry: Immunodeficiency 14 Genetic Testing Registry: Immunodeficiency 36 Activated PI3K-delta ...
    https://medlineplus.gov/.../condition/activated-pi3k-delta-syndrome - Genetics
  2. X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia 
    ... signaling and leads to a novel human primary immunodeficiency. Magnes Res. 2011 Sep;24(3):S109-14. doi: 10.1684/mrh.2011.0286. Citation on PubMed or Free article on PubMed Central Wolf FI, Trapani V. MagT1: a highly ... 10.1684/mrh.2011.0288. Citation on PubMed
    https://medlineplus.gov/...pstein-barr-virus-infection-and-neoplasia - Genetics
  3. Atopic dermatitis 
    ... ClinicalTrials.gov DERMATITIS, ATOPIC DERMATITIS, ATOPIC, 2; ATOD2 IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS; IMD11B PubMed Bieber T. Atopic dermatitis. N Engl J Med. 2008 Apr 3;358(14):1483-94. doi: 10.1056/NEJMra074081. No abstract ...
    https://medlineplus.gov/genetics/condition/atopic-dermatitis - Genetics
  4. T-cell immunodeficiency, congenital alopecia, and nail dystrophy 
    ... A lesson for unraveling complex aspects of novel immunodeficiencies from the human equivalent of the nude/SCID phenotype. J Hematother Stem Cell Res. 2002 Apr;11(2):409-14. doi: 10.1089/152581602753658592. Citation on PubMed Vigliano ...
    https://medlineplus.gov/...cy-congenital-alopecia-and-nail-dystrophy - Genetics
  5. Bare lymphocyte syndrome type II 
    ... Mutation in the Class II Transactivator Associated with Immunodeficiency and Autoimmunity. J Clin Immunol. 2015 Aug;35(6):521-2. doi: 10.1007/s10875-015-0183-z. Epub 2015 Aug 14. No abstract available. Citation on PubMed Burd AL, ...
    https://medlineplus.gov/.../bare-lymphocyte-syndrome-type-ii - Genetics
  6. JAK3-deficient severe combined immunodeficiency 
    JAK3-deficient severe combined immunodeficiency (SCID) is an inherited disorder of the immune system. Individuals with JAK3-deficient SCID lack the necessary ...
    https://medlineplus.gov/...eficient-severe-combined-immunodeficiency - Genetics
  7. Griscelli syndrome 
    ... signs and symptoms of the condition. GS Hypopigmentation immunodeficiency disease Partial albinism with immunodeficiency Genetic Testing Registry: Griscelli syndrome type 1 Genetic ...
    https://medlineplus.gov/genetics/condition/griscelli-syndrome - Genetics
  8. Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome 
    ... conditions are classified as IPEX-like syndromes. Autoimmunity-immunodeficiency syndrome, X-linked Diabetes mellitus, congenital insulin-dependent, ... hemolytic anemia and polyendocrinopathy IDDM-secretory diarrhea syndrome ... polyendocrinopathy, and enteropathy, X-linked Insulin-dependent diabetes ...
    https://medlineplus.gov/...ocrinopathy-enteropathy-x-linked-syndrome - Genetics
  9. Nijmegen breakage syndrome 
    ... Nijmegen breakage syndrome have a malfunctioning immune system (immunodeficiency) with abnormally low levels of immune system proteins ... growth (proliferation) is thought to lead to the immunodeficiency seen in individuals with Nijmegen breakage syndrome. A ...
    https://medlineplus.gov/.../condition/nijmegen-breakage-syndrome - Genetics
  10. Complement component 2 deficiency 
    ... system to malfunction, resulting in a form of immunodeficiency. Immunodeficiencies are conditions in which the immune system is ... and associated infections. Mol Immunol. 2011 Aug;48(14):1643-55. doi: 10.1016/j.molimm.2011. ...
    https://medlineplus.gov/.../complement-component-2-deficiency - Genetics
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