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Summary Literature (0)
DOID:0080669 - posterior polymorphous corneal dystrophy 4

Disease Ontology Definition:A posterior polymorphous corneal dystrophy that is characterized by an irregular posterior corneal surface with occasional opacities of variable size and shape and that has_material_basis_in heterozygous mutation in the GRHL2 gene on chromosome 8q22.

Synonyms:

Xenbase Genes : grhl2


MIM:
MIM:618031 - CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4; PPCD4

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), posterior polymorphous corneal dystrophy (is_a)