Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Congenital hypogonadotropic hypogonadism
0.020 GeneticVariation disease BEFREE R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism. 23936060 2013
Congenital hypogonadotropic hypogonadism
0.020 Biomarker disease BEFREE For more than three decades, GNRH1 was an obvious candidate gene for nCHH in human beings. 20887715 2010