severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive

Rare Disease

MONDO:0011086

Also known as:

SCID due to complete RAG1-2 deficiencySCID due to complete RAG1/2 deficiencysevere combined immunodeficiency due to complete RAG1-2 deficiency

A rare, genetic T-B- severe combined immunodeficiency disorder due to null mutations in recombination activating gene (RAG) 1 and/or RAG2 resulting in less than 1% of wild type V(D)J recombination act...

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severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive

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