Deafness, autosomal dominant nonsyndromic sensorineural 17 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538050
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Deafness, autosomal dominant nonsyndromic sensorineural 17 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MYH9 myosin, heavy chain 9, non-muscle 2.88009