acinar dysplasia caused by mutation in FGFR2
MONDO:0600018Mondo
Findings
No curated finding names acinar dysplasia caused by mutation in FGFR2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any acinar dysplasia in which the cause of the disease is a mutation in the FGFR2 gene.
Definition from the Mondo Disease Ontology (MONDO:0600018), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- FGFR2HGNC:3689
- Limited · PanelApp Australia · Autosomal recessive · 2025
Where it sits
- A kind of
Other names
2 names
Resolves to: acinar dysplasia caused by mutation in FGFR2
- Also called
- FGFR2 acinar dysplasiaFGFR2 related acinar dysplasia