Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4549
Gene Symbol: RNR1
RNR1
CUI: C0011053
Disease: Deafness
Deafness 		0.300 Biomarker CTD_human Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss. 15722487

2005
Entrez Id: 4549
Gene Symbol: RNR1
RNR1
CUI: C0011053
Disease: Deafness
Deafness 		0.300 Biomarker CTD_human Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene. 12031626

2002
Entrez Id: 4549
Gene Symbol: RNR1
RNR1
CUI: C0011053
Disease: Deafness
Deafness 		0.300 Biomarker CTD_human Aminoglycoside-induced hearing loss in a patient with the 961 mutation in mitochondrial DNA. 12037390

2002
Entrez Id: 4549
Gene Symbol: RNR1
RNR1
CUI: C0011053
Disease: Deafness
Deafness 		0.300 Biomarker CTD_human Familial streptomycin ototoxicity in a South African family: a mitochondrial disorder. 9391883

1997