# hypogonadotropic hypogonadism 23 with or without anosmia

> hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the LHB gene on chromosome 19q13

**Wikidata**: [Q9390597](https://www.wikidata.org/wiki/Q9390597)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Fertile_eunuch_syndrome)  
**Source**: https://4ort.xyz/entity/hypogonadotropic-hypogonadism-23-with-or-without-anosmia


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Hypogonadism Caused by a Single Amino Acid Substitution in the β Subunit of Luteinizing Hormone
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)