Hearing Loss, Conductive Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of vibrational conductance of sound to the inner ear leading to impairment of sensory perception of sound. (Human Phenotype Ontology, HP_0000405)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006314
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1 genes/proteins associated with the disease Hearing Loss, Conductive from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
EYA1 EYA transcriptional coactivator and phosphatase 1 2.88009