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DOID:0110855 - posterior polymorphous corneal dystrophy 1
Disease Ontology Definition:A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23.
Synonyms: Ched1, Corneal Endothelial Dystrophy 1, Autosomal Dominant, Maumenee Corneal Dystrophy, Ppcd1,
Echinobase Genes :
MIM:122000 - corneal dystrophy, posterior polymorphous, 1; ppcd1 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee