Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26235
Gene Symbol: FBXL4
FBXL4
0.110 GeneticVariation phenotype BEFREE Mutations in FBXL4 have recently been recognized to cause a mitochondrial disorder, with clinical features including early onset lactic acidosis, hypotonia, and developmental delay. 27743463 2017
Entrez Id: 26235
Gene Symbol: FBXL4
FBXL4
0.110 GeneticVariation phenotype CLINVAR A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13. 27182039 2016
Entrez Id: 26235
Gene Symbol: FBXL4
FBXL4
0.110 Biomarker phenotype HPO