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Results 1 - 10 of 19 for SCID
  1. X-linked severe combined immunodeficiency (SCID) is an inherited disorder of the immune system that occurs almost exclusively in males. Children with X-linked SCID are prone ...
  2. JAK3-deficient severe combined immunodeficiency (SCID) is an inherited disorder of the immune system. Individuals with JAK3-deficient SCID lack the necessary immune cells to fight off ...
  3. ... the immune system and causes severe combined immunodeficiency (SCID). People with SCID lack virtually all immune protection from bacteria, viruses, ... Most individuals with ADA deficiency are diagnosed with SCID in the first 6 months of life. Without ...
  4. ... dystrophy is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized by ... bacteria and viruses. People with this form of SCID are missing functional immune cells called T cells, ...
  5. ... complex class II deficiency MHC class II deficiency SCID due to absence of class II HLA antigens SCID, HLA class 2-negative SCID, HLA class II-negative Severe combined immunodeficiency due ...
  6. ZAP70-related severe combined immunodeficiency (SCID) is an inherited disorder that damages the immune system. ZAP70-related SCID is one of several forms of severe combined immunodeficiency, ...
  7. ... one of several forms of severe combined immunodeficiency (SCID), a group of disorders that cause individuals to ... protection from bacteria, viruses, and fungi. Individuals with SCID are prone to repeated and persistent infections that ...
  8. ... in people with X-linked severe combined immunodeficiency (SCID). This condition is an inherited disorder of the ... Most of the variants that cause X-linked SCID involve changes in one or a few DNA ...
  9. ... severe neural tube defect in human athymic Nude/SCID fetus. Clin Genet. 2008 Apr;73(4):380- ... P, Pignata C. Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation. J Neurol Sci. ...
  10. ... condition is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized by ... of the RAG1 protein cause a form of SCID that is associated with few or no B ...
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