Disease: Ovarian Insufficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1401084
Disease: Ovarian Insufficiency
Ovarian Insufficiency 		0.010 GeneticVariation disease BEFREE The findings also suggest that the N-terminal missense mutation in CLPP does not cause substantial mitochondrial dysfunction or contribute to ovarian insufficiency in an oligogenic manner. 29240891 2018