Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 112812
Gene Symbol: FDX2
FDX2
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		0.710 GeneticVariation UNIPROT A novel complex neurological phenotype due to a homozygous mutation in FDX2. 30010796

2018
Entrez Id: 112812
Gene Symbol: FDX2
FDX2
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		0.710 GeneticVariation UNIPROT We suggest adding genetic analysis of FDX1L in cases of mitochondrial myopathy especially when associated with reduced activity of the respiratory chain complexes I, II and III. 24281368

2014