# hypogonadotropic hypogonadism 20 with or without anosmia

> hypogonadotropic hypogonadism that has material basis in heterozygous mutation in the FGF17 gene on chromosome 8p21, sometimes in association with mutations in other genes

**Wikidata**: [Q30989165](https://www.wikidata.org/wiki/Q30989165)  
**Source**: https://4ort.xyz/entity/hypogonadotropic-hypogonadism-20-with-or-without-anosmia


## References

1. Disease Ontology
2. UniProt
3. Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29