Congenital hypogonadotropic hypogonadism

Part of

Sub-types of Congenital hypogonadotropic hypogonadism

• Combined pituitary hormone deficiencies, genetic form 1 trial · 42 incl. sub-types
  9 sub-types

  • Isolated congenital growth hormone deficiency 38 trials Sub-types →
  • Panhypopituitarism 2 trials Sub-types →
  • Congenital isolated adrenocorticotropic hormone deficiency 1 trial
  • Pituitary hormone deficiency, combined, 1 1 trial
  • Septooptic dysplasia 1 trial Sub-types →
  • Non-acquired combined pituitary hormone deficiency with spine abnormalities 0 trials
  • Pituitary hormone deficiency, combined or isolated, 8 0 trials
  • Pituitary hormone deficiency, combined, 6 0 trials
  • Short stature-pituitary and cerebellar defects-small sella turcica syndrome 0 trials
• Prader-Willi syndrome 32 trials
  5 sub-types

  • Prader-Willi syndrome due to imprinting mutation 0 trials
  • Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 0 trials
  • Prader-Willi syndrome due to paternal 15q11q13 deletion 0 trials Sub-types →
  • Prader-Willi syndrome due to translocation 0 trials
  • Schaaf-Yang syndrome 0 trials
• CHARGE syndrome 4 trials
  1 sub-type

  • CHD7-related CHARGE syndrome 0 trials
• Hypogonadotropic hypogonadism 7 with or without anosmia 3 trials
• Arhinia, choanal atresia, and microphthalmia 1 trial
• Obesity due to congenital leptin deficiency 1 trial
• Obesity due to leptin receptor gene deficiency 1 trial
• Obesity due to prohormone convertase I deficiency 1 trial
• Isolated congenital hypogonadotropic hypogonadism 0 trials · 1 incl. sub-types
  1 sub-type

  • Congenital isolated adrenocorticotropic hormone deficiency 1 trial
• ANE syndrome 0 trials
• Kallmann syndrome-heart disease syndrome 0 trials
• Laurence-Moon syndrome 0 trials
• Martsolf syndrome 1 0 trials
• Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome 0 trials
• Prader-Willi-like syndrome 0 trials
  3 sub-types

  • 6q16 deletion syndrome 0 trials
  • BDV syndrome 0 trials
  • SIM1-related Prader-Willi-like syndrome 0 trials
• Woodhouse-Sakati syndrome 0 trials
• X-linked adrenal hypoplasia congenita 0 trials
  1 sub-type

  • Adrenal hypoplasia, cytomegalic type 0 trials
• Ataxia-hypogonadism-choroidal dystrophy syndrome 0 trials
• Brachytelephalangy-dysmorphism-Kallmann syndrome 0 trials
• Cerebellar ataxia-hypogonadism syndrome 0 trials
  1 sub-type

  • Cerebellar ataxia and hypergonadotropic hypogonadism 0 trials
• Familial adrenal hypoplasia with absent pituitary luteinizing hormone 0 trials
• Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome 0 trials
• Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome 0 trials
• Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome 0 trials
• Polyendocrine-polyneuropathy syndrome 0 trials