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Up to: Hypogonadotropic hypogonadism · Non-acquired pituitary hormone deficiency

Congenital hypogonadotropic hypogonadism

Congenital hypogonadotropic hypogonadism (CHH) is a rare disorder of sexual maturation characterized by gonadotropin (Gn) deficiency with low sex steroid levels associated with low levels of follicle stimulating hormone (FSH) and luteinizing hormone (LH).

0 trials tagged with this condition →

Combined pituitary hormone deficiencies, genetic form 1 trial · 42 incl. sub-types Sub-types →
Prader-Willi syndrome 31 trials Sub-types →
CHARGE syndrome 4 trials Sub-types →
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 Sub-types →
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 Sub-types →
Woodhouse-Sakati syndrome 0 trials
X-linked adrenal hypoplasia congenita 0 trials Sub-types →
Ataxia-hypogonadism-choroidal dystrophy syndrome 0 trials
Brachytelephalangy-dysmorphism-Kallmann syndrome 0 trials
Cerebellar ataxia-hypogonadism syndrome 0 trials Sub-types →
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