Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia
0.110 GeneticVariation disease BEFREE The relatively high incidence of likely NOA-causing mutations in MEIOB that was found in our cohort supports the idea that a complete screening of this gene might be beneficial for clinical evaluation of NOA patients. 30838384 2019
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia
0.110 Biomarker disease HPO