CCMCOPXDN anterior segment dysgenesisPXDN-related ocular dysgenesisanterior segment dysgenesis 7anterior segment dysgenesis 7, with sclerocorneaanterior segment dysgenesis caused by mutation in PXDNsclerocornea with other ocular anomaliesASGD7COPOAcongenital cataract microcornea with corneal opacitycorneal opacification and other ocular anomaliescorneal opacification with Other ocular anomaliescorneal opacification with other ocular anomaliessclerocornea with Other ocular anomalies
Definition
Any anterior segment dysgenesis in which the cause of the disease is a mutation in the PXDN gene.
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