Recombinase activating gene 2 deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
recombinase activating gene 2 deficiency
EFO_0009651
RAG2 Causal
16960852 30046960
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Recombinase activating gene 2 deficiency.
5 View disease cluster →
Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive 1 shared geneRAG2 Related via 1 shared gene including RAG2. Combined cellular and humoral immune defects with granulomas 1 shared geneRAG2 Related via 1 shared gene including RAG2. Salla disease 1 shared geneRAG2 Related via 1 shared gene including RAG2. Combined immunodeficiency with granulomatosis 1 shared geneRAG2 Related via 1 shared gene including RAG2. T-B- severe combined immunodeficiency 1 shared geneRAG2 Related via 1 shared gene including RAG2.