Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6010
Gene Symbol: RHO
RHO
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
Night Blindness, Congenital Stationary, Autosomal Dominant 1 		0.900 GeneticVariation UNIPROT A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness. 9888392

1999
Entrez Id: 6010
Gene Symbol: RHO
RHO
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
Night Blindness, Congenital Stationary, Autosomal Dominant 1 		0.900 GeneticVariation UNIPROT Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation. 7846071

1995
Entrez Id: 6010
Gene Symbol: RHO
RHO
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
Night Blindness, Congenital Stationary, Autosomal Dominant 1 		0.900 GeneticVariation UNIPROT Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness. 8107847

1994
Entrez Id: 6010
Gene Symbol: RHO
RHO
CUI: C1864869
Disease: Night Blindness, Congenital Stationary, Autosomal Dominant 1
Night Blindness, Congenital Stationary, Autosomal Dominant 1 		0.900 GeneticVariation UNIPROT Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. 8358437

1993