sclerocornea
corneal disease in which the cornea blends with sclera, resulting in clouding of the cornea
corneal opacification and other ocular anomalies
sclerocornea that has material basis in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25 and is characterized by corneal opacifiaction, cataract, microcornea, microphthalmia, and anterior segment dysgenesis