Disease: DEAFNESS, AUTOSOMAL DOMINANT 70 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4310775
Disease: DEAFNESS, AUTOSOMAL DOMINANT 70
DEAFNESS, AUTOSOMAL DOMINANT 70 		0.700 GeneticVariation disease UNIPROT Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family. 26196677 2015
CUI: C4310775
Disease: DEAFNESS, AUTOSOMAL DOMINANT 70
DEAFNESS, AUTOSOMAL DOMINANT 70 		0.700 Biomarker disease CLINGEN Whole Exome Sequencing Identified MCM2 as a Novel Causative Gene for Autosomal Dominant Nonsyndromic Deafness in a Chinese Family. 26196677 2015
CUI: C4310775
Disease: DEAFNESS, AUTOSOMAL DOMINANT 70
DEAFNESS, AUTOSOMAL DOMINANT 70 		0.700 Biomarker disease CTD_human
CUI: C4310775
Disease: DEAFNESS, AUTOSOMAL DOMINANT 70
DEAFNESS, AUTOSOMAL DOMINANT 70 		0.700 CausalMutation disease CLINVAR