Gene: GFM2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84340
Gene Symbol: GFM2
GFM2 		0.310 GeneticVariation disease BEFREE These findings suggest that GFM2 mutations could be causative of a phenotype of Leigh syndrome with arthrogryposis multiplex congenita. 26016410 2015
Entrez Id: 84340
Gene Symbol: GFM2
GFM2 		0.310 Biomarker disease GENOMICS_ENGLAND Compound heterozygous GFM2 mutations with Leigh syndrome complicated by arthrogryposis multiplex congenita. 26016410 2015