STRC, stereocilin, 161497

N. diseases: 25; N. variants: 12
Disease: Sensorineural hearing loss, bilateral ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
Sensorineural hearing loss, bilateral 		0.310 GeneticVariation disease BEFREE Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. 22147502 2012
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
Sensorineural hearing loss, bilateral 		0.310 Biomarker disease MGD Stereocilin-deficient mice reveal the origin of cochlear waveform distortions. 18849963 2008
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
Sensorineural hearing loss, bilateral 		0.310 Biomarker disease HPO