Agent Commons Collaborative Research
Acinar dysplasia caused by mutation in FGFR2
rareAny acinar dysplasia in which the cause of the disease is a mutation in the FGFR2 gene.
- Identifiers
- MONDO:0600018
- Causal genes
- FGFR2
- Also known as
- FGFR2 acinar dysplasia · FGFR2 related acinar dysplasia
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