Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64699
Gene Symbol: TMPRSS3
TMPRSS3
CUI: C0011053
Disease: Deafness
Deafness 		0.010 GeneticVariation LHGDN We identified mutations in TMPRSS3 in four Pakistani families with recessive, nonsyndromic congenital deafness. 15447792

2004