Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271582
Disease: Isolated lutropin deficiency (disorder)
Isolated lutropin deficiency (disorder) 		0.700 Biomarker CTD_human

Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.420 Therapeutic CTD_human Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism. 18449926

2008
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.420 Biomarker CTD_human Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism. 18449926

2008
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.420 Biomarker CTD_human Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene. 15602022

2004
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.420 Therapeutic CTD_human Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene. 15602022

2004
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.420 Therapeutic CTD_human Failure of combined follicle-stimulating hormone-testosterone administration to initiate and/or maintain spermatogenesis in men with hypogonadotropic hypogonadism. 8263139

1993
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.420 Biomarker CTD_human Failure of combined follicle-stimulating hormone-testosterone administration to initiate and/or maintain spermatogenesis in men with hypogonadotropic hypogonadism. 8263139

1993
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.420 Therapeutic CTD_human Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. 1727547

1992
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		0.420 Biomarker CTD_human Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. 1727547

1992
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		0.350 Therapeutic CTD_human Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism. 18449926

2008
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		0.350 Biomarker CTD_human Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism. 18449926

2008
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		0.350 Biomarker CTD_human Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene. 15602022

2004
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		0.350 Therapeutic CTD_human Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene. 15602022

2004
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		0.350 Biomarker CTD_human Failure of combined follicle-stimulating hormone-testosterone administration to initiate and/or maintain spermatogenesis in men with hypogonadotropic hypogonadism. 8263139

1993
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		0.350 Therapeutic CTD_human Failure of combined follicle-stimulating hormone-testosterone administration to initiate and/or maintain spermatogenesis in men with hypogonadotropic hypogonadism. 8263139

1993
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		0.350 Therapeutic CTD_human Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. 1727547

1992
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		0.350 Biomarker CTD_human Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. 1727547

1992
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.340 Biomarker CTD_human Altered aquaporin expression in women with polycystic ovary syndrome: hyperandrogenism in follicular fluid inhibits aquaporin-9 in granulosa cells through the phosphatidylinositol 3-kinase pathway. 20378617

2010
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.340 Biomarker CTD_human Troglitazone, an insulin-sensitizing thiazolidinedione, represses combined stimulation by LH and insulin of de novo androgen biosynthesis by thecal cells in vitro. 11889176

2002
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0023601
Disease: Leydig Cell Tumor
Leydig Cell Tumor 		0.300 Biomarker CTD_human Carcinogenicity in rats of the SGLT2 inhibitor canagliflozin. 25289773

2014
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C1136382
Disease: Sclerocystic Ovaries
Sclerocystic Ovaries 		0.300 Biomarker CTD_human Altered aquaporin expression in women with polycystic ovary syndrome: hyperandrogenism in follicular fluid inhibits aquaporin-9 in granulosa cells through the phosphatidylinositol 3-kinase pathway. 20378617

2010
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0034013
Disease: Precocious Puberty
Precocious Puberty 		0.300 Biomarker CTD_human Update on the etiology, diagnosis and therapeutic management of sexual precocity. 18345393

2008
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0271527
Disease: Cryptogenic sexual precocity
Cryptogenic sexual precocity 		0.300 Biomarker CTD_human Update on the etiology, diagnosis and therapeutic management of sexual precocity. 18345393

2008
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0342543
Disease: Central Precocious Puberty
Central Precocious Puberty 		0.300 Biomarker CTD_human Update on the etiology, diagnosis and therapeutic management of sexual precocity. 18345393

2008
Entrez Id: 3972
Gene Symbol: LHB
LHB
CUI: C0948896
Disease: Primary hypogonadism
Primary hypogonadism 		0.300 Biomarker CTD_human Cryptic 17q22 deletion in a boy with a t(10;17)(p15.3;q22) translocation, multiple synostosis syndrome 1, and hypogonadotropic hypogonadism. 18449926

2008