posterior polymorphous corneal dystrophy
GPTKB entity
Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:corneal_dystrophy
genetic disorder |
| gptkbp:affects |
gptkb:Descemet's_membrane
cornea corneal endothelium |
| gptkbp:complication |
secondary glaucoma
|
| gptkbp:diagnosedBy |
slit lamp examination
|
| gptkbp:gene |
gptkb:ZEB1
COL8A2 |
| https://www.w3.org/2000/01/rdf-schema#label |
posterior polymorphous corneal dystrophy
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
122000
|
| gptkbp:onset |
childhood
early adulthood |
| gptkbp:otherName |
gptkb:PPCD
|
| gptkbp:prevalence |
rare
|
| gptkbp:symptom |
blurred vision
asymptomatic corneal edema |
| gptkbp:treatment |
astronomer
corneal transplantation |
| gptkbp:bfsParent |
gptkb:ZEB1
gptkb:COL8A1 |
| gptkbp:bfsLayer |
7
|