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Bare lymphocyte syndrome type 1
- The RFXANK gene provides instructions for making a protein that primarily helps control the activity (transcription) of genes called major histocompatibility ...
- 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 ...
- ... the TAP2 gene have been found to cause bare lymphocyte syndrome type I (BLS I). This immune system disorder often ...
- ... immunodeficiency, congenital alopecia, and nail dystrophy is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized ...
- ... disorder called Omenn syndrome. This condition is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized ... 74 RNF74 V(D)J recombination-activating protein 1 Tests of RAG1 ... PubMed SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-NEGATIVE, ...
- ... disorder called Omenn syndrome. This condition is a type of severe combined immunodeficiency (SCID), which is a group of disorders characterized ...
- ... the gene have been found to cause a type of severe combined immunodeficiency (SCID) known as immunodeficiency 11. SCID is a ...
- ... IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review. Genet Med. 2004 Jan-Feb;6(1):16-26. doi: 10.1097/01.GIM.0000105752. ...
- ZAP70-related severe combined immunodeficiency (SCID) is an inherited disorder that damages the immune system. ZAP70-related SCID is one of several forms ...
- ... SCID from all genetic causes combined is approximately 1 in 50,000, although it may be ... the growth and maturation of certain types of white blood cells (lymphocytes) called T cells ...