COCH, cochlin, 1690

N. diseases: 45; N. variants: 14
Disease: Profound sensorineural hearing loss ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss 		0.010 GeneticVariation disease BEFREE The aim of the study was to search for COCH gene mutations (P51S, V66G, G87W, G88E, V104del, I109N, W117R, A119T, M512T, C542Y) in patients with severe or profound sensorineural hearing loss accompanied by a vestibular lesion. 29765451 2018