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

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