# hypogonadotropic hypogonadism 5 with or without anosmia

> hypogonadotropic hypogonadism that is characterised by autosomal dominant inheritance and has material basis in heterozygous mutation in the CHD7 gene on chromosome 8q12

**Wikidata**: [Q32038857](https://www.wikidata.org/wiki/Q32038857)  
**Source**: https://4ort.xyz/entity/hypogonadotropic-hypogonadism-5-with-or-without-anosmia


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000171316/MONDO_0012880)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)