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Disease Ontology Browser
posterior polymorphous corneal dystrophy 3 (DOID:0110857)
Alliance: disease page
Synonyms: Ppcd3
Alt IDs: OMIM:609141, ICD10CM:H18.50
Definition: A posterior polymorphous corneal dystrophy that has_material_basis_in heterozygous mutation in the ZEB1 gene on chromosome 10p11.22.


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
04/09/2024
MGI 6.23
The Jackson Laboratory