Disease: Eye Diseases, Hereditary ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015398
Disease: Eye Diseases, Hereditary
Eye Diseases, Hereditary 		0.300 Biomarker group CTD_human INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse. 19668215 2009