# Meckel syndrome 6

> Meckel syndrome that has material basis in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32

**Wikidata**: [Q50349685](https://www.wikidata.org/wiki/Q50349685)  
**Source**: https://4ort.xyz/entity/meckel-syndrome-6


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)