Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 17 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the SPRY4 gene.
- Identifiers
- MONDO:0014102 OMIM:615266
- Causal genes
- SPRY4
- Part of
- Kallmann syndrome
- Also known as
- HH17 · hypogonadotropic hypogonadism caused by mutation in SPRY4 · SPRY4 hypogonadotropic hypogonadism
Projects
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