Disease: DEAFNESS, AUTOSOMAL RECESSIVE 97 ×
Source: CURATED ×
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 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