Gene: ERCC5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2073
Gene Symbol: ERCC5
ERCC5 		0.300 GermlineCausalMutation disease ORPHANET A novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis--further evidence of genotype-phenotype correlation. 24700531 2014