inflammatory skin and bowel disease, neonatal, 2 (MONDO_0014481) is any neonatal inflammatory skin and bowel disease in which the cause of the disease is a mutation in the EGFR gene. Also known as: EGFR neonatal inflammatory skin and bowel disease, inflammatory skin and bowel disease, neonatal, type 2, neonatal inflammatory skin and bowel disease caused by mutation in EGFR.