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: 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