# Warburg micro syndrome 3

> Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB18 gene on chromosome 10p12

**Wikidata**: [Q32140486](https://www.wikidata.org/wiki/Q32140486)  
**Source**: https://4ort.xyz/entity/warburg-micro-syndrome-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Loss-of-function mutations in RAB18 cause Warburg micro syndrome.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)