Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 16 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the SEMA3A gene.
- Identifiers
- MONDO:0013961 OMIM:614897
- Causal genes
- SEMA3A
- Part of
- Kallmann syndrome
- Also known as
- HH16 · hypogonadotropic hypogonadism caused by mutation in SEMA3A · SEMA3A hypogonadotropic hypogonadism
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