Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 11 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the TACR3 gene.
- Identifiers
- MONDO:0013913 OMIM:614840
- Causal genes
- TACR3
- Part of
- Kallmann syndrome
- Also known as
- HH11 · hypogonadotropic hypogonadism caused by mutation in TACR3 · TACR3 hypogonadotropic hypogonadism
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