Source: ALL

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 GeneticVariation BEFREE Our results show that after the GJB2 gene mutation in LRTOMT gene is the second cause of congenital hearing impairment in Moroccan patients. 23053991

2012
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
Entrez Id: 220074
Gene Symbol: LRTOMT
LRTOMT
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.430 GeneticVariation LHGDN Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. 18953341

2008
Entrez Id: 220074
Gene Symbol: LRTOMT
LRTOMT
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.430 GeneticVariation BEFREE Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4. 17166180

2007
Entrez Id: 220074
Gene Symbol: LRTOMT
LRTOMT
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.430 GeneticVariation CLINVAR