IL7R-associated SCID

IL7R-associated SCID is a T-, B+, NK+ SCID (MIM.608971) caused by mutation in the IL7R gene (146661) on 5p13, the CD45 gene (MIM.151460) on 1q31-q32, or the CD3D gene (MIM.186790) on 11q23.

See also

 severe combined immunodeficiency (SCID)

• recessive SCID
  • JAK3-associated SCID
  • IL7R-associated SCID
  • T-, B-, NK- SCID (102700) caused by mutation in the ADA (608958) gene on 20q13.11 (ADA-associated SCID)
  • T-, B-, NK+ SCID with sensitivity to ionizing radiation caused by mutation in the Artemis gene on 10p;
  • T-, B-, NK+ SCID caused by mutation in the RAG1 and RAG2 genes on 11p13 (RAGs-associated SCID)

Approximately 20 to 30% of all SCID patients are T-, B-, NK+, and approximately half of these patients have mutations in the RAG1 or RAG2 genes (RAGs-associated SCID)