(Q3513968)
English
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
- sclerocornea with other ocular anomalies
- anterior segment dysgenesis
Statements
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Identifiers
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Sitelinks
Wikipedia(1 entry)
- frwiki Taie cornéenne