Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 14 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the WDR11 gene.
- Identifiers
- MONDO:0013926 OMIM:614858
- Causal genes
- WDR11
- Part of
- Kallmann syndrome
- Also known as
- HH14 · hypogonadotropic hypogonadism caused by mutation in WDR11 · WDR11 hypogonadotropic hypogonadism
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