Isolated lutropin deficiency (disorder)
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone.
|
1727547 |
1992 |
Isolated lutropin deficiency (disorder)
|
0.700 |
Biomarker
|
disease |
CTD_human |
|
|
|
Isolated lutropin deficiency (disorder)
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
Isolated lutropin deficiency (disorder)
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Isolated lutropin deficiency (disorder)
|
0.700 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
Hypogonadotropic hypogonadism
|
0.420 |
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 |
Hypogonadotropic hypogonadism
|
0.420 |
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 |
Hypogonadotropic hypogonadism
|
0.420 |
GeneticVariation
|
disease |
BEFREE |
Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations: mutant DAX-1 failed to repress steroidogenic acute regulatory protein (StAR) and luteinizing hormone beta-subunit gene promoter activity.
|
18202527 |
2008 |
Hypogonadotropic hypogonadism
|
0.420 |
AlteredExpression
|
disease |
BEFREE |
There was no effect of the allelic variant of the luteinizing hormone beta-subunit gene on luteinizing hormone levels in patients with hypogonadotropic hypogonadism as compared to healthy subjects.
|
16358135 |
2005 |
Hypogonadotropic hypogonadism
|
0.420 |
Biomarker
|
disease |
CTD_human |
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
|
15602022 |
2004 |
Hypogonadotropic hypogonadism
|
0.420 |
Therapeutic
|
disease |
CTD_human |
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
|
15602022 |
2004 |
Hypogonadotropic hypogonadism
|
0.420 |
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 |
Hypogonadotropic hypogonadism
|
0.420 |
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 |
Hypogonadotropic hypogonadism
|
0.420 |
Therapeutic
|
disease |
CTD_human |
Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone.
|
1727547 |
1992 |
Hypogonadotropic hypogonadism
|
0.420 |
Biomarker
|
disease |
CTD_human |
Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone.
|
1727547 |
1992 |
Hypogonadotropic hypogonadism
|
0.420 |
Biomarker
|
disease |
HPO |
|
|
|
Hypogonadism
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
We identified a novel mutation in the LHB gene in a male patient with hypogonadism and provided evidence that LHB nonsense mutation can cause selective LH deficiency.
|
29476300 |
2018 |
Hypogonadism
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
Inactivating Luteinizing hormone beta (LHB) gene mutations are exceptionally rare and lead to hypogonadism that is particularly severe in males.
|
27656125 |
2016 |
Hypogonadism
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
Hypogonadism in a patient with two novel mutations of the luteinizing hormone β-subunit gene expressed in a compound heterozygous form.
|
22723313 |
2012 |
Hypogonadism
|
0.350 |
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 |
Hypogonadism
|
0.350 |
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 |
Hypogonadism
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
Selective luteinizing hormone deficiency due to mutations in the luteinizing hormone beta-subunit gene (LHB) is a rare cause of hypogonadism.
|
17761593 |
2007 |
Hypogonadism
|
0.350 |
Biomarker
|
disease |
CTD_human |
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
|
15602022 |
2004 |
Hypogonadism
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
|
15602022 |
2004 |
Hypogonadism
|
0.350 |
Therapeutic
|
disease |
CTD_human |
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
|
15602022 |
2004 |