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Idiopathic Hypogonadotropic Hypogonadism [Supplementary Concept]

A hereditary autosomal recessive type of hypogonadism characterized by absent or incomplete sexual maturation by age 18 and low levels of circulating GONADOTROPINS and TESTOSTERONE and no other abnormalities of the hypothalamic-pituitary axis. Nonreproductive phenotypes, such as ANOSMIA; CLEFT PALATE, and SENSORINEURAL HEARING LOSS may also occur. Mutations in the GNRHR gene (gonadotropin-releasing hormone receptor) have been identified for HH7. OMIM: 146110

Date introduced: November 5, 2012

MeSH Unique ID: C562785

Heading Mapped to:

Entry Terms:

  • Hypogonadotropic Hypogonadism 7 With Or Without Anosmia
  • HH7

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