posterior amorphous corneal dystrophy (DOID:0060452)
Alliance: disease page
Synonyms: chromosome 12q21.33 deletion syndrome; PACD
Alt IDs: OMIM:612868, ICD10CM:H18.5, MESH:C567546, ORDO:98971
Definition: 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.