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 		0.110 GeneticVariation disease BEFREE Our results suggest that GZF1 mutations cause a phenotype of severe myopia and significant articular involvement not previously described in Larsen syndrome. 28475863 2017
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.110 Biomarker disease HPO