Disease: Retinal Degeneration ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration 		0.500 Biomarker phenotype CTD_human Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration. 22842230 2012
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration 		0.500 Biomarker phenotype MGD