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Items: 2

1.

Thinning of Descemet membrane

A reduction in the thickness of Descemet's membrane. [from HPO]

MedGen UID:
1376185
Concept ID:
C4477011
Finding
2.

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

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