Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8022
Gene Symbol: LHX3
LHX3
0.430 Biomarker disease BEFREE Considering genotype/phenotype correlation, we suggest that the presence of SNHL and limited neck rotation should be considered in the differential diagnosis of CPHD3 to facilitate molecular diagnosis. 28302169 2017
Entrez Id: 8022
Gene Symbol: LHX3
LHX3
0.430 GeneticVariation disease BEFREE LHX3 mutations are associated with growth hormone, prolactin, gonadotropin, and TSH deficiency; abnormal pituitary morphology; and may be accompanied with limited neck rotation and sensorineural hearing loss. 21249393 2011
Entrez Id: 8022
Gene Symbol: LHX3
LHX3
0.430 GeneticVariation disease BEFREE This study therefore extends the phenotypic spectrum associated with LHX3 mutations to encompass variable sensorineural hearing loss and suggests a possible interaction between LHX3 and SOX2 likely to be important for development of both the inner ear and the anterior pituitary in human embryonic development. 18407919 2008
Entrez Id: 8022
Gene Symbol: LHX3
LHX3
0.430 GeneticVariation disease LHGDN This study therefore extends the phenotypic spectrum associated with LHX3 mutations to encompass variable sensorineural hearing loss and suggests a possible interaction between LHX3 and SOX2 likely to be important for development of both the inner ear and the anterior pituitary in human embryonic development. 18407919 2008
Entrez Id: 8022
Gene Symbol: LHX3
LHX3
0.430 Biomarker disease GENOMICS_ENGLAND This study therefore extends the phenotypic spectrum associated with LHX3 mutations to encompass variable sensorineural hearing loss and suggests a possible interaction between LHX3 and SOX2 likely to be important for development of both the inner ear and the anterior pituitary in human embryonic development. 18407919 2008
Entrez Id: 8022
Gene Symbol: LHX3
LHX3
0.430 Biomarker disease HPO