Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 3 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the PROKR2 gene.
- Identifiers
- MONDO:0009482 OMIM:244200
- Causal genes
- PROKR2
- Part of
- Kallmann syndrome
- Also known as
- HH3 · hypogonadotropic hypogonadism caused by mutation in PROKR2 · KAL3 · Kallmann syndrome 3 · PROKR2 hypogonadotropic hypogonadism
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