Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
MELAS Syndrome
CUI: C0162671
Disease: MELAS Syndrome
0.700 GeneticVariation CLINVAR Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus. 7726154 1995
Mitochondrial Diseases
CUI: C0751651
Disease: Mitochondrial Diseases
0.700 CausalMutation CLINVAR
MYOPATHY, MITOCHONDRIAL, WITH DIABETES MELLITUS
CUI: C4016608
Disease: MYOPATHY, MITOCHONDRIAL, WITH DIABETES MELLITUS
0.700 CausalMutation CLINVAR
Diabetes-deafness syndrome maternally transmitted (disorder)
CUI: C0342289
Disease: Diabetes-deafness syndrome maternally transmitted (disorder)
0.700 CausalMutation CLINVAR