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Disease Ontology Browser
posterior polymorphous corneal dystrophy (DOID:0060457)
Alliance: disease page
Synonyms: hereditary polymorphus posterior corneal dystrophy; PPCD; Schlichting dystrophy
Alt IDs: ICD10CM:H18.5, MESH:C562745, OMIM:PS122000, ORDO:98973
Definition: A corneal dystrophy that is characterised by changes in Descemet's membrane and endothelial layer.

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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last database update
MGI 6.22
The Jackson Laboratory