CABP2, calcium binding protein 2, 51475

N. diseases: 6; N. variants: 2
Disease: Severe sensorineural hearing impairment ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4021533
Disease: Severe sensorineural hearing impairment
Severe sensorineural hearing impairment 		0.010 GeneticVariation disease BEFREE We show that genetic defects in CABP2 cause moderate-to-severe sensorineural hearing impairment. 22981119 2012