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inflammatory skin and bowel disease, neonatal, 2

Disease Summary
Associated Targets (1)


Mondo Description Any neonatal inflammatory skin and bowel disease in which the cause of the disease is a mutation in the EGFR gene.
Uniprot Description A disorder characterized by inflammatory features with neonatal onset, involving the skin, hair, and gut. The skin lesions involve perioral and perianal erythema, psoriasiform erythroderma, with flares of erythema, scaling, and widespread pustules. Gastrointestinal symptoms include malabsorptive diarrhea that is exacerbated by intercurrent gastrointestinal infections. The hair is short or broken, and the eyelashes and eyebrows are wiry and disorganized.
Mondo Term and Equivalent IDs
MONDO:0014481:  inflammatory skin and bowel disease, neonatal, 2