C203453Level 10
Severe Combined Immunodeficiency due to RAG Deficiency
**Semantic type:** Disease or Syndrome
**Definition:** A rare severe combined immunodeficiency disorder caused by null mutations in recombination activating gene (RAG) 1 or RAG2. It is associated with a lack of T and B cells.
**Synonyms:** - Severe Combined Immunodeficiency with RAG Deficiency
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