Disease: Congenital hypogonadotropic hypogonadism ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3899503
Disease: Congenital hypogonadotropic hypogonadism
Congenital hypogonadotropic hypogonadism 		0.020 Biomarker disease BEFREE Congenital hypogonadotropic hypogonadism/Kallmann Syndrome (CHH/KS) is a rare condition characterized by gonadotropin deficiency and pubertal failure. 31770102 2020
CUI: C3899503
Disease: Congenital hypogonadotropic hypogonadism
Congenital hypogonadotropic hypogonadism 		0.020 Biomarker disease BEFREE Congenital hypogonadotropic hypogonadism/Kallmann syndrome (CHH/KS) is a rare, treatable form of infertility. 31333578 2019