OTOGL, otogelin like, 283310

N. diseases: 9; N. variants: 8
Disease: Sensorineural Hearing Loss (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.030 GeneticVariation disease BEFREE Mutations affecting the OTOGL gene have been recently connected with nonsyndromic sensorineural hearing loss. 28426234 2017
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.030 GeneticVariation disease BEFREE Novel biallelic OTOGL mutations in a Chinese family with moderate non-syndromic sensorineural hearing loss. 25829320 2015
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.030 GeneticVariation disease BEFREE We propose that OTOGL mutations affect the production and/or function of acellular structures of the inner ear, which ultimately leads to sensorineural hearing loss. 23122586 2012