Disease: DEAFNESS, AUTOSOMAL RECESSIVE 97 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4084709
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 97
DEAFNESS, AUTOSOMAL RECESSIVE 97 		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
CUI: C4084709
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 97
DEAFNESS, AUTOSOMAL RECESSIVE 97 		0.510 GeneticVariation disease UNIPROT A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss. 25941349 2015
CUI: C4084709
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 97
DEAFNESS, AUTOSOMAL RECESSIVE 97 		0.510 Biomarker disease CTD_human