Any congenital alveolar dysplasia in which the cause of the disease is a mutation in the FGF10 gene.
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ventricular septal defect
MONDO:0002070
hypoplastic left heart syndrome
MONDO:0004933
familial cardiomyopathy
MONDO:0005217
atrial septal defect
MONDO:0006664
familial bicuspid aortic valve
MONDO:0007194
Alagille syndrome
MONDO:0007318