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Hypogonadotropic hypogonadism 1 with or without anosmia
rareThe X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3.
- Identifiers
- MONDO:0010635 OMIM:308700
- Causal genes
- ANOS1
- Part of
- Kallmann syndrome
- Also known as
- ANOS1 hypogonadotropic hypogonadism · HH1 · hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive · hypogonadotropic hypogonadism caused by mutation in ANOS1 · KAL1
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