Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 4 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the PROK2 gene.
- Identifiers
- MONDO:0012528 OMIM:610628
- Causal genes
- PROK2
- Part of
- Kallmann syndrome
- Also known as
- HH4 · hypogonadotropic hypogonadism caused by mutation in PROK2 · Kallmann syndrome 4 · PROK2 hypogonadotropic hypogonadism
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