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 		0.300 Biomarker phenotype CTD_human In addition, the finding of rare heterozygous QRX sequence changes in three individuals with retinal degeneration raises the possibility that QRX may be involved in disease pathogenesis. 15028672 2004