# Catel–Manzke syndrome

> Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia, cleft palate and glossoptosis

**Wikidata**: [Q5051865](https://www.wikidata.org/wiki/Q5051865)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Catel–Manzke_syndrome)  
**Source**: https://4ort.xyz/entity/catel-manzke-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. UniProt
3. Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000088451/MONDO_0014507)