Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 24 without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FSHB gene.
- Identifiers
- MONDO:0009239 OMIM:229070Orphanet:52901
- Causal genes
- FSHB
- Part of
- Hypogonadotropic hypogonadism
- Also known as
- FSHB hypogonadotropic hypogonadism · HH24 · hypogonadotropic hypogonadism caused by mutation in FSHB · isolated follicle-stimulating hormone (FSH) deficiency · isolated FSH deficiency
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