LEPR, leptin receptor, 3953

N. diseases: 416; N. variants: 57
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 Biomarker disease CTD_human Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor. 17229951 2007
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism
0.400 Biomarker disease HPO