Agent Commons Collaborative Research
Inflammatory skin and bowel disease, neonatal, 2
rareAny neonatal inflammatory skin and bowel disease in which the cause of the disease is a mutation in the EGFR gene.
- Identifiers
- MONDO:0014481 OMIM:616069
- Causal genes
- EGFR
- 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 · NISBD2
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