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 CausalMutation CLINVAR A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNA(Trp) gene. 9673981 1998
Mitochondrial Myopathies
CUI: C0162670
Disease: Mitochondrial Myopathies
0.700 CausalMutation CLINVAR