# C syndrome

> C syndrome is a rare multiple congenital anomaly/intellectual disability syndrome characterized by trigonocephaly and metopic suture synostosis, dysmorphic facial features, short neck, skeletal anomalies, and variable intellectual disability

**Wikidata**: [Q1022312](https://www.wikidata.org/wiki/Q1022312)  
**Source**: https://4ort.xyz/entity/c-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)