RHO, rhodopsin, 6010

N. diseases: 178; N. variants: 71
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1864877
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B (disorder) 		0.300 Biomarker disease CTD_human Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. 8358437 1993