Disease: Metamorphopsia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0271185
Disease: Metamorphopsia
Metamorphopsia 		0.300 Biomarker phenotype CTD_human tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. 18711368 2008