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GENATLAS PHENOTYPE
last update : 25/08/2006
Symbol OBS1
Location 7q32.1
Name severe early-onset obesity
Corresponding gene LEP
Main clinical features leptin deficiency, (hypogonadotropic hypogonadism)
Genetic determination
Function/system disorder metabolism/carbohydrates
Type disease
Gene product
Name congenital deficiency of leptin (LEP)
Remark(s)