Disease: Pseudohypopyon ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pseudohypopyon
CUI: C4068898
Disease: Pseudohypopyon
0.010 GeneticVariation BEFREE The one proband with compound heterozygous variants (p.S7N and p.R218H) exhibited typical BVMD phenotypes (pseudohypopyon stage and vitelliruptive stage in the right and left eyes, respectively). 26201355 2015