DISEASES

Disease-gene associations mined from literature

Human genes for cone-rod dystrophy

Cone-rod dystrophy [DOID:0050572]

A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain.

Synonyms:  cone-rod dystrophy,  conerod dystrophy,  DOID:0050572,  cone-rod dystrophy 5,  cone-rod retinal dystrophy ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17 #18 #19 #20