# Warburg micro syndrome

> autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism

**Wikidata**: [Q6839205](https://www.wikidata.org/wiki/Q6839205)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Warburg_Micro_syndrome)  
**Source**: https://4ort.xyz/entity/warburg-micro-syndrome


## References

1. Disease Ontology
2. Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome
3. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000115839/Orphanet_2510)
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000099246/Orphanet_2510)
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000118873/Orphanet_2510)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000125875/Orphanet_2510)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)