# Warburg micro syndrome 2

> Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP2 gene on chromosome 1q41

**Wikidata**: [Q32140475](https://www.wikidata.org/wiki/Q32140475)  
**Source**: https://4ort.xyz/entity/warburg-micro-syndrome-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)