# Meckel syndrome

> a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia.

**Wikidata**: [Q1915681](https://www.wikidata.org/wiki/Q1915681)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Meckel–Gruber_syndrome)  
**Source**: https://4ort.xyz/entity/meckel-syndrome


## References

1. Disease Ontology
2. Freebase Data Dumps. 2013
3. MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome
4. YSO-Wikidata mapping project
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)