Disease: Corneal dystrophy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Corneal dystrophy
CUI: C0010036
Disease: Corneal dystrophy
0.700 GeneticVariation CLINVAR Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4. 29499165 2018