Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23562
Gene Symbol: CLDN14
CLDN14
CUI: C3279660
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 29
DEAFNESS, AUTOSOMAL RECESSIVE 29 		0.900 Biomarker GENOMICS_ENGLAND Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss. 22246673

2012
Entrez Id: 23562
Gene Symbol: CLDN14
CLDN14
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.400 Biomarker GENOMICS_ENGLAND Given the known involvement of CLDN14 gene in NSHL, DNA samples from hearing-impaired members from the four families were sequenced to potentially identify causal variants within this gene. 22246673

2012