# Charcot-Marie-Tooth disease type 2R

> Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or compound heterozygous mutation in the TRIM2 gene on chromosome 4q

**Wikidata**: [Q27164468](https://www.wikidata.org/wiki/Q27164468)  
**Source**: https://4ort.xyz/entity/charcot-marie-tooth-disease-type-2r


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)