Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
0.300 Biomarker disease CLINGEN Leigh map: A novel computational diagnostic resource for mitochondrial disease. 27977873 2017
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
0.300 Biomarker disease CLINGEN New insights into the phenotype of FARS2 deficiency. 29126765 2017
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
0.300 Biomarker disease CLINGEN A Newly Identified Missense Mutation in FARS2 Causes Autosomal-Recessive Spastic Paraplegia. 26553276 2016
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
0.300 Biomarker disease CLINGEN Novel Compound Heterozygous Mutations Expand the Recognized Phenotypes of FARS2-Linked Disease. 27095821 2016
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
0.300 Biomarker disease CLINGEN Clinical findings in a patient with FARS2 mutations and early-infantile-encephalopathy with epilepsy. 27549011 2016
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
0.300 Biomarker disease CLINGEN Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy. 22833457 2012
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
0.300 Biomarker disease CLINGEN Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes. 22499341 2012