PCDH9, protocadherin 9, 5101

N. diseases: 35; N. variants: 14
Disease: Auditory neuropathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1852271
Disease: Auditory neuropathy
Auditory neuropathy 		0.010 GeneticVariation disease BEFREE Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1). 19353688 2009