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Hypogonadotropic hypogonadism 18 with or without anosmia
rareAny hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the IL17RD gene.
- Identifiers
- MONDO:0014103 OMIM:615267
- Causal genes
- IL17RD
- Part of
- Kallmann syndrome
- Also known as
- HH18 · hypogonadotropic hypogonadism 18 with or without anosmia, Autosomal recessive, Autosomal dominant, Digenic dominant · hypogonadotropic hypogonadism caused by mutation in IL17RD · IL17RD hypogonadotropic hypogonadism
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