SAG, S-antigen visual arrestin, 6295

N. diseases: 97; N. variants: 9
Disease: Cone-rod synaptic disorder, congenital nonprogressive ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4041558
Disease: Cone-rod synaptic disorder, congenital nonprogressive
Cone-rod synaptic disorder, congenital nonprogressive 		0.300 Biomarker disease CTD_human A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese. 7670478 1995