mutations in KDM6A or KMT2D have been identified in Kabuki syndrome, and mutations in genes implicated in primary immunodeficiencies (TNFRSF6, CTLA4, STAT3, PIK3CD, CBL, ADAR1, LRBA, RAG1, and KRAS) have been reported in 40% of Evans syndrome patients, an association of AIHA and ITP....