Hüpogonadotroopne hüpogonadism
Munasarjade või munandite talitlushäire, mis tuleneb hüpotalamus-hüpofüüsi telje ebapiisavast hormonaalsest stimulatsioonist.
Analüüsitud geenid
Tuntud ka nimetustena
central hypogonadism; congenital idiopathic hypogonadotropic hypogonadism; gonadotropic deficiency; hypogonadism, hypogonadotropic; hypogonadotropic hypogonadism with or without anosmia; hypogonadotropism; isolated congenital gonadotropin deficiency; low gonadotropins (secondary hypogonadism); nIHH; normosmic congenital hypogonadotropic hypogonadism; Normosmic idiopathic hypogonadotropic hypogonadism; secondary hypogonadism
Hõlmab 87 seotud alatüüpi ↓Peida alatüübid ↑
- 6q16 deletion syndrome
- adrenal hypoplasia, cytomegalic type
- ANE syndrome
- arhinia, choanal atresia, and microphthalmia
- ataxia-hypogonadism-choroidal dystrophy syndrome
- BDV syndrome
- brachytelephalangy-dysmorphism-Kallmann syndrome
- cerebellar ataxia and hypergonadotropic hypogonadism
- cerebellar ataxia-hypogonadism syndrome
- CHARGE syndrome
- CHD7-related CHARGE syndrome
- combined pituitary hormone deficiencies, genetic form
- congenital absence of septum pellucidum
- congenital hypogonadotropic hypogonadism
- congenital isolated adrenocorticotropic hormone deficiency
- familial adrenal hypoplasia with absent pituitary luteinizing hormone
- hypogonadotropic hypogonadism 1 with or without anosmia
- hypogonadotropic hypogonadism 10 with or without anosmia
- hypogonadotropic hypogonadism 11 with or without anosmia
- hypogonadotropic hypogonadism 12 with or without anosmia
- hypogonadotropic hypogonadism 13 with or without anosmia
- hypogonadotropic hypogonadism 14 with or without anosmia
- hypogonadotropic hypogonadism 15 with or without anosmia
- hypogonadotropic hypogonadism 16 with or without anosmia
- hypogonadotropic hypogonadism 17 with or without anosmia
- hypogonadotropic hypogonadism 18 with or without anosmia
- hypogonadotropic hypogonadism 19 with or without anosmia
- hypogonadotropic hypogonadism 2 with or without anosmia
- hypogonadotropic hypogonadism 20 with or without anosmia
- hypogonadotropic hypogonadism 21 with or without anosmia
- hypogonadotropic hypogonadism 22 with or without anosmia
- hypogonadotropic hypogonadism 23 with or without anosmia
- hypogonadotropic hypogonadism 24 without anosmia
- hypogonadotropic hypogonadism 25 with anosmia
- hypogonadotropic hypogonadism 26 with or without anosmia
- hypogonadotropic hypogonadism 27 without anosmia
- hypogonadotropic hypogonadism 3 with or without anosmia
- hypogonadotropic hypogonadism 4 with or without anosmia
- hypogonadotropic hypogonadism 5 with or without anosmia
- hypogonadotropic hypogonadism 6 with or without anosmia
- hypogonadotropic hypogonadism 7 with or without anosmia
- hypogonadotropic hypogonadism 8 with or without anosmia
- hypogonadotropic hypogonadism 9 with or without anosmia
- hypogonadotropic hypogonadism-frontoparietal alopecia syndrome
- hypogonadotropic hypogonadism-retinitis pigmentosa syndrome
- hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome
- isolated congenital growth hormone deficiency
- isolated congenital hypogonadotropic hypogonadism
- isolated growth hormone deficiency type IA
- isolated growth hormone deficiency type IB
- isolated growth hormone deficiency type II
- isolated growth hormone deficiency type III
- isolated growth hormone deficiency, type 4
- isolated growth hormone deficiency, type 5
- Kallmann syndrome
- Kallmann syndrome-heart disease syndrome
- Laurence-Moon syndrome
- Martsolf syndrome 1
- Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome
- non-acquired combined pituitary hormone deficiency with spine abnormalities
- obesity due to congenital leptin deficiency
- obesity due to leptin receptor gene deficiency
- obesity due to prohormone convertase I deficiency
- pagon stephan syndrome
- panhypopituitarism
- panhypopituitarism, X-linked
- pituitary hormone deficiency, combined or isolated, 8
- pituitary hormone deficiency, combined, 1
- pituitary hormone deficiency, combined, 2
- pituitary hormone deficiency, combined, 6
- polyendocrine-polyneuropathy syndrome
- Prader-Willi syndrome
- Prader-Willi syndrome due to imprinting mutation
- Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
- Prader-Willi syndrome due to paternal 15q11q13 deletion
- Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
- Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
- Prader-Willi syndrome due to translocation
- Prader-Willi-like syndrome
- Schaaf-Yang syndrome
- septooptic dysplasia
- short stature due to growth hormone qualitative anomaly
- short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
- short stature-pituitary and cerebellar defects-small sella turcica syndrome
- SIM1-related Prader-Willi-like syndrome
- Woodhouse-Sakati syndrome
- X-linked adrenal hypoplasia congenita
