hypogonadotropic hypogonadism 23 with or without anosmia (Q9390597)

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A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13.
  • Hypogonadism with spermatogenesis
  • PASQUALINI SYNDROME
  • Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency
  • 46,XY disorder of sex development due to LHB deficiency
  • 46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency
  • leydig cell hypoplasia due to LHB deficiency
  • 46,XY DSD due to luteinizing hormone subunit beta deficiency
  • fertile eunuch syndrome
  • 46,XY DSD due to LHB deficiency
  • HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA
  • HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23
  • HH23
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Language Label Description Also known as
English
hypogonadotropic hypogonadism 23 with or without anosmia
A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13.
  • Hypogonadism with spermatogenesis
  • PASQUALINI SYNDROME
  • Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency
  • 46,XY disorder of sex development due to LHB deficiency
  • 46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency
  • leydig cell hypoplasia due to LHB deficiency
  • 46,XY DSD due to luteinizing hormone subunit beta deficiency
  • fertile eunuch syndrome
  • 46,XY DSD due to LHB deficiency
  • HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA
  • HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23
  • HH23

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