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Hypogonadotropic hypogonadism 12 with or without anosmia
rareA hypogonadotropic hypogonadism that has material basis in homozygous mutation in the GNRH1 gene on chromosome 8p21.
- Identifiers
- MONDO:0013914 OMIM:227200OMIM:614841
- Part of
- Hypogonadotropic hypogonadism
- Also known as
- eunuchoidism familial hypogonadotropic · eunuchoidism, familial hypogonadotropic · familial hypogonadotropic eunuchoidism · FIGD · gonadotropin deficiency familial idiopathic
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