A severe combined immunodeficiency that is the result of a mutation on Chromosome 6 RAG2 gene involving genetic rearrangement of both the T- and B-lymphocyte receptor genes.
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recombinase activating gene 1 deficiency
MONDO:0000572
janus kinase-3 deficiency
MONDO:0005511
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
MONDO:0011132
T-B- severe combined immunodeficiency
MONDO:0017855
severe combined immunodeficiency due to CARMIL2 deficiency
MONDO:0029134
immunodeficiency 79
MONDO:0030981