Gene: LHB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3972
Gene Symbol: LHB
LHB 		0.300 Biomarker disease 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 		0.300 Therapeutic disease 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 		0.300 Therapeutic disease 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 		0.300 Biomarker disease 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 		0.300 Therapeutic disease 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 		0.300 Biomarker disease 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 		0.300 Therapeutic disease 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 		0.300 Biomarker disease CTD_human Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone. 1727547 1992