MEIOB, meiosis specific with OB-fold, 254528

N. diseases: 14; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004509
Disease: Azoospermia
Azoospermia
0.120 GeneticVariation disease BEFREE Therefore, the relative incidence of MEIOB mutations in azoospermia should be further assessed in larger and diverse cohorts in order to determine the efficiency of MEIOB sequence screening for clinical evaluations. 30838384 2019
CUI: C0004509
Disease: Azoospermia
Azoospermia
0.120 GeneticVariation disease BEFREE We identified three novel likely causative mutations of azoospermia in three genes: MEIOB, TEX14, and DNAH6. 28206990 2017
CUI: C0004509
Disease: Azoospermia
Azoospermia
0.120 Biomarker disease HPO