posterior polymorphous corneal dystrophy

Summary

DOID:0060457 - posterior polymorphous corneal dystrophy

Disease Ontology Definition:A corneal dystrophy that is characterised by changes in Descemet's membrane and endothelial layer.

Synonyms: PPCD, Schlichting dystrophy, hereditary polymorphus posterior corneal dystrophy

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: zeb1, grhl2, vsx1, ovol2, col8a2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0020364 - posterior polymorphous corneal dystrophy

MONDO:0020364 - posterior polymorphous corneal dystrophy

OMIM:

OMIM:122000 - CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1; PPCD1
OMIM:609141 - CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3; PPCD3

OMIM:122000 - CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1; PPCD1

OMIM:609141 - CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3; PPCD3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): corneal dystrophy (is_a), corneal endothelial dystrophy (is_a)