CD3E, CD3e molecule, 916

N. diseases: 73; N. variants: 4
Disease: Omenn Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2700553
Disease: Omenn Syndrome
Omenn Syndrome 		0.310 GeneticVariation disease BEFREE Here we show the effect of anti-CD3ε mAb administration in the RAG2(R229Q) mouse model, which closely recapitulates human OS. 22723555 2012
CUI: C2700553
Disease: Omenn Syndrome
Omenn Syndrome 		0.310 Biomarker disease CTD_human Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3. 15546002 2004