Anterior segment dysgenesis 7

Any anterior segment dysgenesis in which the cause of the disease is a mutation in the PXDN gene.

Also known as: CCMCO, PXDN anterior segment dysgenesis, PXDN-related ocular dysgenesis, anterior segment dysgenesis 7, anterior segment dysgenesis 7, with sclerocornea, anterior segment dysgenesis caused by mutation in PXDN, sclerocornea with other ocular anomalies, ASGD7

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