Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Idiopathic hypogonadotropic hypogonadism
0.010 GeneticVariation disease BEFREE These findings also contribute structural information to understand mutations in human 6-OST isoform 1 associated with the human genetic disease idiopathic hypogonadotropic hypogonadism characterized by incomplete or lack of puberty. 28103688 2017