Source: GENOMICS_ENGLAND

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 Biomarker GENOMICS_ENGLAND 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 Biomarker GENOMICS_ENGLAND 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