(Q30989609)
English
hypogonadotropic hypogonadism 12 with or without anosmia
hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21
- familial hypogonadotrophic eunuchoidism
- familial idiopathic gonadotrpin deficiency
- FIGD
- Eunuchoidism, Familial Hypogonadotropic
- HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA
- Eunuchoidism familial hypogonadotropic
- Gonadotropin deficiency familial idiopathic
- Familial hypogonadotropic eunuchoidism
- HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA; HH12
- Gonadotropin Deficiency, Familial Idiopathic
- HH12
Statements
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