# Mowat-Wilson syndrome

> rare genetic disorder

**Wikidata**: [Q2757585](https://www.wikidata.org/wiki/Q2757585)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Mowat–Wilson_syndrome)  
**Source**: https://4ort.xyz/entity/mowat-wilson-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. [Source](https://ddrare.nibiohn.go.jp/)
3. Disease Ontology
4. Freebase Data Dumps. 2013
5. UniProt
6. Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease
7. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/cb06ff0d-1cc6-494c-9ce5-f7cb26f34620--2018-05-24T12:34:43)
8. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_cb06ff0d-1cc6-494c-9ce5-f7cb26f34620-2018-05-24T123443.951Z)
9. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000169554/MONDO_0009341)
10. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)