# odontoonychodermal syndrome

> syndrome characterized by craniofacial, neurologic, limb and ocular abnormalities

**Wikidata**: [Q17148148](https://www.wikidata.org/wiki/Q17148148)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Oculodentodigital_dysplasia)  
**Source**: https://4ort.xyz/entity/odontoonychodermal-syndrome


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000152661/MONDO_0008111)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)