Disease: Severe myopia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.120 GeneticVariation disease BEFREE Our results provide additional evidence to support the idea that mutation in LRPAP1 is associated with high myopia. 25525168 2014
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.120 GeneticVariation disease BEFREE Mutations in LRPAP1 are associated with severe myopia in humans. 23830514 2013
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.120 Biomarker disease HPO