TRNE, tRNA, 4556

N. diseases: 83; N. variants: 4
Disease: Ataxia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004134
Disease: Ataxia
Ataxia 		0.110 GeneticVariation phenotype BEFREE Early-onset cataracts, spastic paraparesis, and ataxia caused by a novel mitochondrial tRNAGlu (MT-TE) gene mutation causing severe complex I deficiency: a clinical, molecular, and neuropathologic study. 23334599 2013
CUI: C0004134
Disease: Ataxia
Ataxia 		0.110 Biomarker phenotype HPO