Disease: hearing impairment ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.400 Biomarker phenotype GENOMICS_ENGLAND New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p. 9286457 1997
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.400 CausalMutation phenotype CLINVAR