# Meier-Gorlin syndrome

> autosomal recessive disorder characterized by severe intrauterine and postnatal growth retardation, microcephaly, bilateral microtia and hypoplastic patellae

**Wikidata**: [Q19587381](https://www.wikidata.org/wiki/Q19587381)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Meier-Gorlin_syndrome)  
**Source**: https://4ort.xyz/entity/meier-gorlin-syndrome


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000085840/Orphanet_2554)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000091651/Orphanet_2554)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000093009/Orphanet_2554)
8. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000094804/Orphanet_2554)
9. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000115947/Orphanet_2554)
10. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000167513/Orphanet_2554)
11. [Identifiers.org](https://registry.identifiers.org/registry/doid)