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secondary hypogonadism
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
GNRHR
GNRH1
NSMF
KISS1R
PRDM13
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
REACTOME_CLASS_A1_RHODOPSIN_LIKE_RECEPTORS
MATZUK_CENTRAL_FOR_FEMALE_FERTILITY
ovulation cycle
REACTOME_G_ALPHA_Q_SIGNALLING_EVENTS
REACTOME_GASTRIN_CREB_SIGNALLING_PATHWAY_VIA_PKC_AND_MAPK
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Curated Studies
Most Correlated Studies
OMIM - Boucher-Neuhauser syndrome
OMIM - Hypogonadism disorder
OMIM - Disorder of eye
Mouse Phenotypes - Disease of anterior pituitary
OMIM - Hypogonadism
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Literature
Most Relevant Literature
Approach to the patient with hypogonadotropic hypogonadism.
Male acquired hypogonadotropic hypogonadism: diagnosis and treatment.
Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism.
Approach to the male patient with congenital hypogonadotropic hypogonadism.
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
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Clinical Trials
Most Relevant Clinical Trials
Study to Evaluate the Safety and Efficacy of Androxal Treatment in Men With Secondary Hypogonadism
Study to Evaluate the Safety and Efficacy of Androxalâ„¢ Treatment in Men With Secondary Hypogonadism
Safety Study of Enclomiphene Citrate in the Treatment of Men With Secondary Hypogonadism
Normalization of Morning Testosterone Levels in Men With Secondary Hypogonadism
To Evaluate Sperm Parameters in Men With Secondary Hypogonadism Previously Treated With Topical Test…
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