# Warburg micro syndrome 4

> Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the TBC1D20 gene on chromosome 20p13

**Wikidata**: [Q32140499](https://www.wikidata.org/wiki/Q32140499)  
**Source**: https://4ort.xyz/entity/warburg-micro-syndrome-4


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)