Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.350 Therapeutic CTD_human Phenotypic effects of leptin replacement on morbid obesity, diabetes mellitus, hypogonadism, and behavior in leptin-deficient adults. 15070752

2004
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.350 Biomarker CTD_human Phenotypic effects of leptin replacement on morbid obesity, diabetes mellitus, hypogonadism, and behavior in leptin-deficient adults. 15070752

2004
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.350 Therapeutic CTD_human A leptin missense mutation associated with hypogonadism and morbid obesity. 9500540

1998
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.350 Biomarker CTD_human A leptin missense mutation associated with hypogonadism and morbid obesity. 9500540

1998