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Congenital alveolar dysplasia due to FGF10

MONDO:0100090

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

Also known as: CAD due to FGF10

66 clinical trials for this condition and its sub-types.

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Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Congenital heart disease (248) Hereditary disease (176) Human disease (14) Congenital anomaly of cardiovascular system (5) Cardiogenetic disease (3) Disease of genetic or genomic mechanism (2) Congenital alveolar dysplasia (0)
Trials to join now! 31 Not yet recruiting 6 Not yet finished but already full! 10 Completed 18 Terminated 1
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