Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 220074
Gene Symbol: LRTOMT
LRTOMT
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.430 Biomarker GENOMICS_ENGLAND Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. 18953341

2008