Deafness, Autosomal Dominant 25 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:C565319
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Genes

1 genes/proteins associated with the disease Deafness, Autosomal Dominant 25 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8 2.88009