Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 20 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGF17 gene.
- Identifiers
- MONDO:0014106 OMIM:615270
- Causal genes
- FGF17
- Part of
- Kallmann syndrome
- Also known as
- FGF17 hypogonadotropic hypogonadism · HH20 · hypogonadotropic hypogonadism caused by mutation in FGF17
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