Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4233
Gene Symbol: MET
MET 		0.510 GeneticVariation disease BEFREE Mutations in the mesenchymal epithelial transition factor (MET) gene are frequently associated with multiple human cancers but can also lead to human non-syndromic autosomal recessive deafness (DFNB97). 31801140 2019
Entrez Id: 4233
Gene Symbol: MET
MET 		0.510 GeneticVariation disease UNIPROT A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss. 25941349 2015
Entrez Id: 4233
Gene Symbol: MET
MET 		0.510 Biomarker disease CTD_human