Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 2 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGFR1 gene.
- Identifiers
- MONDO:0007844 OMIM:147950
- Causal genes
- FGFR1
- Part of
- Kallmann syndrome
- Also known as
- FGFR1 hypogonadotropic hypogonadism · HH2 · hypogonadotropic hypogonadism caused by mutation in FGFR1 · KAL2
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