# Sensenbrenner syndrome

> Human disease

**Wikidata**: [Q7451019](https://www.wikidata.org/wiki/Q7451019)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Sensenbrenner_syndrome)  
**Source**: https://4ort.xyz/entity/sensenbrenner-syndrome


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_e7e56d33-315b-40a0-9ec5-0a99e12cf369-2021-07-30T130934.464Z)
6. Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)
8. UMLS 2023