# Woodhouse–Sakati syndrome

> Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia

**Wikidata**: [Q8032762](https://www.wikidata.org/wiki/Q8032762)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Woodhouse–Sakati_syndrome)  
**Source**: https://4ort.xyz/entity/woodhouse-sakati-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_6a1d7719-4261-494d-87aa-745518580673-2021-02-19T162051.399Z)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_6a1d7719-4261-494d-87aa-745518580673-2021-07-27T153526.827Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000115827/MONDO_0009419)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)