# Meckel syndrome 3

> Meckel syndrome that has material basis in an autosomal recessive mutation of TMEM67 on chromosome 8q22.1

**Wikidata**: [Q50349682](https://www.wikidata.org/wiki/Q50349682)  
**Source**: https://4ort.xyz/entity/meckel-syndrome-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)