Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 9 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the NSMF gene.
- Identifiers
- MONDO:0013911 OMIM:614838
- Causal genes
- NSMF
- Part of
- Kallmann syndrome
- Also known as
- HH9 · hypogonadotropic hypogonadism caused by mutation in NSMF · NSMF hypogonadotropic hypogonadism
Projects
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