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Posterior polymorphous corneal dystrophy 1
A posterior polymorphous corneal dystrophy that has material basis in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23. [from MONDO]
Abnormal corneal endothelium morphology
Abnormality of the corneal endothelium, that is, the single layer of cells on the inner surface of the cornea. [from HPO]
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