LEP, leptin, 3952

N. diseases: 931; N. variants: 15
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism
0.400 Therapeutic disease CTD_human Phenotypic effects of leptin replacement on morbid obesity, diabetes mellitus, hypogonadism, and behavior in leptin-deficient adults. 15070752 2004
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism
0.400 Biomarker disease CTD_human Phenotypic effects of leptin replacement on morbid obesity, diabetes mellitus, hypogonadism, and behavior in leptin-deficient adults. 15070752 2004
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism
0.400 Therapeutic disease CTD_human A leptin missense mutation associated with hypogonadism and morbid obesity. 9500540 1998
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism
0.400 Biomarker disease CTD_human A leptin missense mutation associated with hypogonadism and morbid obesity. 9500540 1998
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism
0.400 Biomarker disease HPO