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posterior polymorphous corneal dystrophy 2

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any posterior polymorphous corneal dystrophy in which the cause of the disease is a mutation in the COL8A2 gene.
Uniprot Description A rare mild subtype of posterior corneal dystrophy characterized by alterations of Descemet membrane presenting as vesicles, opacities or band-like lesions on slit-lamp examination and specular microscopy. Affected patient typically are asymptomatic.
Mondo Term and Equivalent IDs
MONDO:0012199:  posterior polymorphous corneal dystrophy 2
MESH:C565176: 
UMLS:C1852795: