Human genes for posterior amorphous corneal dystrophy
Posterior amorphous corneal dystrophy [DOID:0060452]
A stromal dystrophy that is characterized by irregular sheetlike areas of opacification with involvement of the Descemet membrane and, in some instances, alterations of the normal endothelial mosaic and that has_material_basis_in a chromosome 12q21.33 contiguous gene deletion syndrome.
Synonyms: posterior amorphous corneal dystrophy, DOID:0060452, posterior amorphous corneal dystrophies, chromosome 12q21.33 deletion syndrome, PACD ...