# ataxia-telangiectasia-like disorder

> autosomal recessive condition caused by mutation(s) in the MRE11A gene, encoding double-strand break repair protein MRE11. It is characterized by progressive cerebellar degeneration resulting in ataxia and oculomotor apraxia

**Wikidata**: [Q55345773](https://www.wikidata.org/wiki/Q55345773)  
**Source**: https://4ort.xyz/entity/ataxia-telangiectasia-like-disorder


## References

1. Monarch Disease Ontology release 2018-06-29
2. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000020922/MONDO_0011457)