congenital alveolar dysplasia due to FGF10
MONDO:0100090Mondo
Findings
No curated finding names congenital alveolar dysplasia due to FGF10 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any congenital alveolar dysplasia in which the cause of the disease is a mutation in the FGF10 gene.
Definition from the Mondo Disease Ontology (MONDO:0100090), 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.
- FGF10HGNC:3666
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
Other names
1 name
Resolves to: congenital alveolar dysplasia due to FGF10
- Also called
- CAD due to FGF10