MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: Nonsyndromic Deafness ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.010 Biomarker disease BEFREE Thus, MYH9 may not currently be a good candidate gene for efficient screening of genetic causes in nonsyndromic deafness. 19645626 2009