Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 15 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the HS6ST1 gene.
- Identifiers
- MONDO:0013946 OMIM:614880
- Causal genes
- HS6ST1
- Part of
- Kallmann syndrome
- Also known as
- HH15 · HS6ST1 hypogonadotropic hypogonadism · hypogonadotropic hypogonadism caused by mutation in HS6ST1
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