Hypogonadotropic Hypogonadism

Alias:

Klinefelter Syndrome

Klinefelter's Syndrome

Xxy Syndrome

Xxy Trisomy

Hypogonadotropism

47, Xxy

Congenital Idiopathic Hypogonadotropic Hypogonadism

Isolated Congenital Gonadotropin Deficiency

Klinefelter Syndrome Karyotype 47, Xxy

Klinefelter Syndrome, Unspecified

Klinefelter Syndrome in Males

Klinefelters Syndrome

47, Xxy Syndrome

47,xxy Syndrome

Hypogonadism

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hypogonadotropic Hypogonadism, also known as klinefelter syndrome, is related to hypogonadotropic hypogonadism 7 with or without anosmia and hypogonadotropic hypogonadism 2 with or without anosmia. An important gene associated with Hypogonadotropic Hypogonadism is FGFR1 (Fibroblast Growth Factor Receptor 1), and among its related pathways/superpathways are GPCR downstream signalling and Signal Transduction. The drugs Dutasteride and Atorvastatin have been mentioned in the context of this disorder. Affiliated tissues include pituitary and testes, and related phenotypes are Increased shRNA abundance (Z-score > 2) and nervous system

Related ID：

MALACARDS：HYP730

MESH：D007713

ICD11：1472503127