World Of Taxonomy
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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