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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

75 clinical trials for this condition and its sub-types, 0 tagged with Congenital alveolar dysplasia due to FGF10 itself.

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Where it sits in the disease tree

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Part of

↑ Cardiogenetic disease (618) ↑ Congenital alveolar dysplasia (0)
Including sub-types (75) Tagged with Congenital alveolar dysplasia due to FGF10 (0)
Trials to join now! 34 Not yet recruiting 12 Not yet finished but already full! 11 Completed 17 Terminated 1
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