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congenital alveolar dysplasia due to FGF10

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Any congenital alveolar dysplasia in which the cause of the disease is a mutation in the FGF10 gene.

Synonyms

  • CAD due to FGF10
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