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Items: 2

1.

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]

MedGen UID:
343836
Concept ID:
C1852555
Disease or Syndrome
2.

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]

MedGen UID:
868921
Concept ID:
C4023332
Anatomical Abnormality

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