Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Striatonigral Degeneration, Infantile, Mitochondrial
0.400 GeneticVariation disease UNIPROT A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosis. 7668837 1995
Striatonigral Degeneration, Infantile, Mitochondrial
0.400 CausalMutation disease CLINVAR