Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 6 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGF8 gene.
- Identifiers
- MONDO:0012988 OMIM:612702
- Causal genes
- FGF8
- Part of
- Kallmann syndrome
- Also known as
- FGF8 hypogonadotropic hypogonadism · HH6 · hypogonadotropic hypogonadism caused by mutation in FGF8 · Kallmann syndrome 6
Projects
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