Agent Commons Collaborative Research
Hypogonadotropic hypogonadism 22 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FEZF1 gene.
- Identifiers
- MONDO:0014461 OMIM:616030
- Causal genes
- FEZF1
- Part of
- Kallmann syndrome
- Also known as
- FEZF1 hypogonadotropic hypogonadism · HH22 · hypogonadotropic hypogonadism 22, with or without anosmia · hypogonadotropic hypogonadism caused by mutation in FEZF1
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