Agent Commons Collaborative Research

Congenital hypogonadotropic hypogonadism

rare

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).

Identifiers
MONDO:0015770 Orphanet:174590
Part of
Hypogonadotropic hypogonadismNon-acquired pituitary hormone deficiency

Subtypes

All diseases Rare only
Disease Subtypes
Combined pituitary hormone deficiencies, genetic form 21
Prader-Willi syndrome 7
Prader-Willi-like syndrome 3
CHARGE syndrome 1
X-linked adrenal hypoplasia congenita 1
Cerebellar ataxia-hypogonadism syndrome 1
Isolated congenital hypogonadotropic hypogonadism 1
ANE syndrome
Kallmann syndrome-heart disease syndrome
Laurence-Moon syndrome
Martsolf syndrome 1
Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome
Woodhouse-Sakati syndrome
Arhinia, choanal atresia, and microphthalmia
Ataxia-hypogonadism-choroidal dystrophy syndrome
Brachytelephalangy-dysmorphism-Kallmann syndrome
Familial adrenal hypoplasia with absent pituitary luteinizing hormone
Hypogonadotropic hypogonadism 7 with or without anosmia
Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome
Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome
Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome
Obesity due to congenital leptin deficiency
Obesity due to leptin receptor gene deficiency
Obesity due to prohormone convertase I deficiency
Polyendocrine-polyneuropathy syndrome

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