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Disease Ontology Browser
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory