Disease: Empty follicle syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1328577
Disease: Empty follicle syndrome
Empty follicle syndrome 		0.030 Biomarker disease BEFREE Although LHCGR and ZP3 were identified as causative genes, it is still unclear what happens to these patients' oocytes, and the pathogenesis of EFS remains obscure. 31734689 2019
CUI: C1328577
Disease: Empty follicle syndrome
Empty follicle syndrome 		0.030 GeneticVariation disease BEFREE Our findings provide researchers and clinicians with a better understanding of phenotype-genotype correlations between EFS and 46, XY DSD and the LHCGR gene. 29912377 2018
CUI: C1328577
Disease: Empty follicle syndrome
Empty follicle syndrome 		0.030 GeneticVariation disease BEFREE Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome. 21683950 2011