Inflammatory skin and bowel disease, neonatal, 2

MONDO:0014481

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, 2, inflammatory skin and bowel disease, neonatal, type 2, neonatal inflammatory skin and bowel disease caused by mutation in EGFR, NISBD2

63 clinical trials for this condition and its sub-types, 0 tagged with Inflammatory skin and bowel disease, neonatal, 2 itself.

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↑ Neonatal inflammatory skin and bowel disease (0)

Including sub-types (63) Tagged with Inflammatory skin and bowel disease, neonatal, 2 (0)

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