Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2796
Gene Symbol: GNRH1
GNRH1
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.260 Biomarker MGD Sertoli cell androgen receptor DNA binding domain is essential for the completion of spermatogenesis. 19574395

2009
Entrez Id: 2796
Gene Symbol: GNRH1
GNRH1
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.260 Biomarker MGD Gonadotrophin-releasing hormone deficiency in a mutant mouse with hypogonadism. 198666

1977