HGF, hepatocyte growth factor, 3082

N. diseases: 671; N. variants: 22
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842342
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder) 		0.600 Biomarker disease GENOMICS_ENGLAND Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss. 27610647 2016
CUI: C1842342
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder) 		0.600 Biomarker disease CTD_human
CUI: C1842342
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder) 		0.600 CausalMutation disease CLINVAR