Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0848765
Disease: Hearing disability
Hearing disability
0.010 GeneticVariation disease BEFREE <i>ILDR1</i>-dependent ARNSHL (DFNB42, OMIM: # 609646) is a very rare sub-type of hearing disability, with unknown prevalence, caused by function-damaging genetic variants in <i>ILDR1</i> gene reported in families of Middle-Eastern origin. 28713423 2017