# hypogonadotropic hypogonadism 14 with or without anosmia

> hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the WDR11 gene on chromosome 10q26

**Wikidata**: [Q30990097](https://www.wikidata.org/wiki/Q30990097)  
**Source**: https://4ort.xyz/entity/hypogonadotropic-hypogonadism-14-with-or-without-anosmia


## References

1. Disease Ontology
2. UniProt
3. WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
4. [Identifiers.org](https://registry.identifiers.org/registry/doid)
5. Monarch Disease Ontology release 2018-06-29