Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Sensorineural Hearing Loss (disorder)
0.410 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
Sensorineural Hearing Loss (disorder)
0.410 Biomarker disease GENOMICS_ENGLAND Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)]. 8741917 1996
Sensorineural Hearing Loss (disorder)
0.410 Biomarker disease HPO