Conditions / Genetic

hypogonadotropic hypogonadism 20 with or without anosmia

info · Genetic · ICD-10: E23.0

A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGF17 gene on chromosome 8p21, sometimes in association with mutations in other genes.

Signs and symptoms

  • Osteopenia
  • Anosmia
  • Delayed puberty
  • Hypogonadism
  • Osteoporosis