Results 1 - 10 of 15 for Bare lymphocyte syndrome type 1
  1. ... condition. HLA class I deficiency Genetic Testing Registry: Bare lymphocyte syndrome type 1 Disease InfoSearch National Organization for Rare Disorders (NORD) ...
  2. The RFXANK gene provides instructions for making a protein that primarily helps control the activity (transcription) of genes called major histocompatibility ...
  3. The TAP1 gene provides instructions for making a protein that plays an important role in the immune system. The TAP1 protein assembles with another protein ...
  4. ... the TAP2 gene have been found to cause bare lymphocyte syndrome type I (BLS I). This immune system disorder often ...
  5. ... immunodeficiency, congenital alopecia, and nail dystrophy is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized ...
  6. ... HUMORAL IMMUNE DEFECTS WITH GRANULOMAS RECOMBINATION-ACTIVATING GENE 1 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, ...
  7. ... disorder called Omenn syndrome. This condition is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized ...
  8. ... the gene have been found to cause a type of severe combined immunodeficiency (SCID) known as immunodeficiency 11. SCID is a ...
  9. ... IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review. Genet Med. 2004 Jan-Feb;6(1):16-26. Review. Citation on PubMed Lebet T, ...
  10. ZAP70-related severe combined immunodeficiency (SCID) is an inherited disorder that damages the immune system. ZAP70-related SCID is one of several forms ...
previous · 1 · 2 · next